SNP for Gene (Select 367) - SNP

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Select item 14915557181.

rs1491555718 has merged into rs113528927 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACACACAC>-,ACAC,ACACAC,ACACACACAC,ACACACACACAC,ACACACACACACAC,ACACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACAC,ACACACACACACACACACACAC [Show Flanks]
Chromosome:: X:67723533 (GRCh38)
X:66943375 (GRCh37)
Canonical SPDI:: NC_000023.11:67723520:ACACACACACACACACACAC:ACACACACACAC,NC_000023.11:67723520:ACACACACACACACACACAC:ACACACACACACACAC,NC_000023.11:67723520:ACACACACACACACACACAC:ACACACACACACACACAC,NC_000023.11:67723520:ACACACACACACACACACAC:ACACACACACACACACACACAC,NC_000023.11:67723520:ACACACACACACACACACAC:ACACACACACACACACACACACAC,NC_000023.11:67723520:ACACACACACACACACACAC:ACACACACACACACACACACACACAC,NC_000023.11:67723520:ACACACACACACACACACAC:ACACACACACACACACACACACACACAC,NC_000023.11:67723520:ACACACACACACACACACAC:ACACACACACACACACACACACACACACAC,NC_000023.11:67723520:ACACACACACACACACACAC:ACACACACACACACACACACACACACACACAC,NC_000023.11:67723520:ACACACACACACACACACAC:ACACACACACACACACACACACACACACACACAC
Gene:: AR (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Clinical significance:: benign,likely-benign
Validated:: by frequency,by alfa,by cluster
MAF:: ACACACACACACACAC=0./0 (ALFA)
ACACACAC=0.1452/548 (1000Genomes)
HGVS:: NC_000023.11:g.67723521AC[6], NC_000023.11:g.67723521AC[8], NC_000023.11:g.67723521AC[9], NC_000023.11:g.67723521AC[11], NC_000023.11:g.67723521AC[12], NC_000023.11:g.67723521AC[13], NC_000023.11:g.67723521AC[14], NC_000023.11:g.67723521AC[15], NC_000023.11:g.67723521AC[16], NC_000023.11:g.67723521AC[17], NC_000023.10:g.66943363AC[6], NC_000023.10:g.66943363AC[8], NC_000023.10:g.66943363AC[9], NC_000023.10:g.66943363AC[11], NC_000023.10:g.66943363AC[12], NC_000023.10:g.66943363AC[13], NC_000023.10:g.66943363AC[14], NC_000023.10:g.66943363AC[15], NC_000023.10:g.66943363AC[16], NC_000023.10:g.66943363AC[17], NG_009014.2:g.184490AC[6], NG_009014.2:g.184490AC[8], NG_009014.2:g.184490AC[9], NG_009014.2:g.184490AC[11], NG_009014.2:g.184490AC[12], NG_009014.2:g.184490AC[13], NG_009014.2:g.184490AC[14], NG_009014.2:g.184490AC[15], NG_009014.2:g.184490AC[16], NG_009014.2:g.184490AC[17]

Select item 14915246832.

rs1491524683 has merged into rs1280599162 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>-,ATAT [Show Flanks]
Chromosome:: X:67604198 (GRCh38)
X:66824040 (GRCh37)
Canonical SPDI:: NC_000023.11:67604195:ATAT:AT,NC_000023.11:67604195:ATAT:ATATAT
Gene:: AR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATAT=0./0 (ALFA)
-=0.00042/2 (1000Genomes)
HGVS:: NC_000023.11:g.67604196AT[1], NC_000023.11:g.67604196AT[3], NC_000023.10:g.66824038AT[1], NC_000023.10:g.66824038AT[3], NG_009014.2:g.65165AT[1], NG_009014.2:g.65165AT[3]

Select item 14915137163.

rs1491513716 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: X:67577005 (GRCh38)
X:66796848 (GRCh37)
Canonical SPDI:: NC_000023.11:67577005::C
Gene:: AR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.00177/21 (ALFA)
C=0.00194/150 (GnomAD)
HGVS:: NC_000023.11:g.67577005_67577006insC, NC_000023.10:g.66796847_66796848insC, NG_009014.2:g.37974_37975insC

Select item 14914805034.

rs1491480503 has merged into rs10666509 [Homo sapiens]

Variant type:: DELINS
Alleles:: TATATATATATATATATATATATATATATATA>-,TA,TATA,TATATA,TATATATA,TATATATATA,TATATATATATA,TATATATATATATA,TATATATATATATATA,TATATATATATATATATA,TATATATATATATATATATA,TATATATATATATATATATATA,TATATATATATATATATATATATA,TATATATATATATATATATATATATA,TATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATATATATA [Show Flanks]
Chromosome:: X:67728584 (GRCh38)
X:66948426 (GRCh37)
Canonical SPDI:: NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:67728574:ATATATATATATATATATATATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA
Gene:: AR (Varview)
Functional Consequence:: 3_prime_UTR_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATATATA=0./0 (ALFA)
HGVS:: NC_000023.11:g.67728576TA[4], NC_000023.11:g.67728576TA[5], NC_000023.11:g.67728576TA[6], NC_000023.11:g.67728576TA[7], NC_000023.11:g.67728576TA[8], NC_000023.11:g.67728576TA[9], NC_000023.11:g.67728576TA[10], NC_000023.11:g.67728576TA[11], NC_000023.11:g.67728576TA[12], NC_000023.11:g.67728576TA[13], NC_000023.11:g.67728576TA[14], NC_000023.11:g.67728576TA[15], NC_000023.11:g.67728576TA[16], NC_000023.11:g.67728576TA[17], NC_000023.11:g.67728576TA[18], NC_000023.11:g.67728576TA[19], NC_000023.11:g.67728576TA[21], NC_000023.11:g.67728576TA[22], NC_000023.11:g.67728576TA[23], NC_000023.11:g.67728576TA[24], NC_000023.11:g.67728576TA[25], NC_000023.11:g.67728576TA[26], NC_000023.11:g.67728576TA[27], NC_000023.11:g.67728576TA[28], NC_000023.11:g.67728576TA[29], NC_000023.11:g.67728576TA[30], NC_000023.11:g.67728576TA[31], NC_000023.11:g.67728576TA[32], NC_000023.10:g.66948418TA[4], NC_000023.10:g.66948418TA[5], NC_000023.10:g.66948418TA[6], NC_000023.10:g.66948418TA[7], NC_000023.10:g.66948418TA[8], NC_000023.10:g.66948418TA[9], NC_000023.10:g.66948418TA[10], NC_000023.10:g.66948418TA[11], NC_000023.10:g.66948418TA[12], NC_000023.10:g.66948418TA[13], NC_000023.10:g.66948418TA[14], NC_000023.10:g.66948418TA[15], NC_000023.10:g.66948418TA[16], NC_000023.10:g.66948418TA[17], NC_000023.10:g.66948418TA[18], NC_000023.10:g.66948418TA[19], NC_000023.10:g.66948418TA[21], NC_000023.10:g.66948418TA[22], NC_000023.10:g.66948418TA[23], NC_000023.10:g.66948418TA[24], NC_000023.10:g.66948418TA[25], NC_000023.10:g.66948418TA[26], NC_000023.10:g.66948418TA[27], NC_000023.10:g.66948418TA[28], NC_000023.10:g.66948418TA[29], NC_000023.10:g.66948418TA[30], NC_000023.10:g.66948418TA[31], NC_000023.10:g.66948418TA[32], NG_009014.2:g.189545TA[4], NG_009014.2:g.189545TA[5], NG_009014.2:g.189545TA[6], NG_009014.2:g.189545TA[7], NG_009014.2:g.189545TA[8], NG_009014.2:g.189545TA[9], NG_009014.2:g.189545TA[10], NG_009014.2:g.189545TA[11], NG_009014.2:g.189545TA[12], NG_009014.2:g.189545TA[13], NG_009014.2:g.189545TA[14], NG_009014.2:g.189545TA[15], NG_009014.2:g.189545TA[16], NG_009014.2:g.189545TA[17], NG_009014.2:g.189545TA[18], NG_009014.2:g.189545TA[19], NG_009014.2:g.189545TA[21], NG_009014.2:g.189545TA[22], NG_009014.2:g.189545TA[23], NG_009014.2:g.189545TA[24], NG_009014.2:g.189545TA[25], NG_009014.2:g.189545TA[26], NG_009014.2:g.189545TA[27], NG_009014.2:g.189545TA[28], NG_009014.2:g.189545TA[29], NG_009014.2:g.189545TA[30], NG_009014.2:g.189545TA[31], NG_009014.2:g.189545TA[32], NM_000044.6:c.*4735TA[4], NM_000044.6:c.*4735TA[5], NM_000044.6:c.*4735TA[6], NM_000044.6:c.*4735TA[7], NM_000044.6:c.*4735TA[8], NM_000044.6:c.*4735TA[9], NM_000044.6:c.*4735TA[10], NM_000044.6:c.*4735TA[11], NM_000044.6:c.*4735TA[12], NM_000044.6:c.*4735TA[13], NM_000044.6:c.*4735TA[14], NM_000044.6:c.*4735TA[15], NM_000044.6:c.*4735TA[16], NM_000044.6:c.*4735TA[17], NM_000044.6:c.*4735TA[18], NM_000044.6:c.*4735TA[19], NM_000044.6:c.*4735TA[21], NM_000044.6:c.*4735TA[22], NM_000044.6:c.*4735TA[23], NM_000044.6:c.*4735TA[24], NM_000044.6:c.*4735TA[25], NM_000044.6:c.*4735TA[26], NM_000044.6:c.*4735TA[27], NM_000044.6:c.*4735TA[28], NM_000044.6:c.*4735TA[29], NM_000044.6:c.*4735TA[30], NM_000044.6:c.*4735TA[31], NM_000044.6:c.*4735TA[32], NM_000044.5:c.*4735TA[4], NM_000044.5:c.*4735TA[5], NM_000044.5:c.*4735TA[6], NM_000044.5:c.*4735TA[7], NM_000044.5:c.*4735TA[8], NM_000044.5:c.*4735TA[9], NM_000044.5:c.*4735TA[10], NM_000044.5:c.*4735TA[11], NM_000044.5:c.*4735TA[12], NM_000044.5:c.*4735TA[13], NM_000044.5:c.*4735TA[14], NM_000044.5:c.*4735TA[15], NM_000044.5:c.*4735TA[16], NM_000044.5:c.*4735TA[17], NM_000044.5:c.*4735TA[18], NM_000044.5:c.*4735TA[19], NM_000044.5:c.*4735TA[21], NM_000044.5:c.*4735TA[22], NM_000044.5:c.*4735TA[23], NM_000044.5:c.*4735TA[24], NM_000044.5:c.*4735TA[25], NM_000044.5:c.*4735TA[26], NM_000044.5:c.*4735TA[27], NM_000044.5:c.*4735TA[28], NM_000044.5:c.*4735TA[29], NM_000044.5:c.*4735TA[30], NM_000044.5:c.*4735TA[31], NM_000044.5:c.*4735TA[32], NM_000044.4:c.*4735TA[4], NM_000044.4:c.*4735TA[5], NM_000044.4:c.*4735TA[6], NM_000044.4:c.*4735TA[7], NM_000044.4:c.*4735TA[8], NM_000044.4:c.*4735TA[9], NM_000044.4:c.*4735TA[10], NM_000044.4:c.*4735TA[11], NM_000044.4:c.*4735TA[12], NM_000044.4:c.*4735TA[13], NM_000044.4:c.*4735TA[14], NM_000044.4:c.*4735TA[15], NM_000044.4:c.*4735TA[16], NM_000044.4:c.*4735TA[17], NM_000044.4:c.*4735TA[18], NM_000044.4:c.*4735TA[19], NM_000044.4:c.*4735TA[21], NM_000044.4:c.*4735TA[22], NM_000044.4:c.*4735TA[23], NM_000044.4:c.*4735TA[24], NM_000044.4:c.*4735TA[25], NM_000044.4:c.*4735TA[26], NM_000044.4:c.*4735TA[27], NM_000044.4:c.*4735TA[28], NM_000044.4:c.*4735TA[29], NM_000044.4:c.*4735TA[30], NM_000044.4:c.*4735TA[31], NM_000044.4:c.*4735TA[32], NM_000044.3:c.*4735TA[4], NM_000044.3:c.*4735TA[5], NM_000044.3:c.*4735TA[6], NM_000044.3:c.*4735TA[7], NM_000044.3:c.*4735TA[8], NM_000044.3:c.*4735TA[9], NM_000044.3:c.*4735TA[10], NM_000044.3:c.*4735TA[11], NM_000044.3:c.*4735TA[12], NM_000044.3:c.*4735TA[13], NM_000044.3:c.*4735TA[14], NM_000044.3:c.*4735TA[15], NM_000044.3:c.*4735TA[16], NM_000044.3:c.*4735TA[17], NM_000044.3:c.*4735TA[18], NM_000044.3:c.*4735TA[19], NM_000044.3:c.*4735TA[21], NM_000044.3:c.*4735TA[22], NM_000044.3:c.*4735TA[23], NM_000044.3:c.*4735TA[24], NM_000044.3:c.*4735TA[25], NM_000044.3:c.*4735TA[26], NM_000044.3:c.*4735TA[27], NM_000044.3:c.*4735TA[28], NM_000044.3:c.*4735TA[29], NM_000044.3:c.*4735TA[30], NM_000044.3:c.*4735TA[31], NM_000044.3:c.*4735TA[32], NM_001011645.3:c.*4735TA[4], NM_001011645.3:c.*4735TA[5], NM_001011645.3:c.*4735TA[6], NM_001011645.3:c.*4735TA[7], NM_001011645.3:c.*4735TA[8], NM_001011645.3:c.*4735TA[9], NM_001011645.3:c.*4735TA[10], NM_001011645.3:c.*4735TA[11], NM_001011645.3:c.*4735TA[12], NM_001011645.3:c.*4735TA[13], NM_001011645.3:c.*4735TA[14], NM_001011645.3:c.*4735TA[15], NM_001011645.3:c.*4735TA[16], NM_001011645.3:c.*4735TA[17], NM_001011645.3:c.*4735TA[18], NM_001011645.3:c.*4735TA[19], NM_001011645.3:c.*4735TA[21], NM_001011645.3:c.*4735TA[22], NM_001011645.3:c.*4735TA[23], NM_001011645.3:c.*4735TA[24], NM_001011645.3:c.*4735TA[25], NM_001011645.3:c.*4735TA[26], NM_001011645.3:c.*4735TA[27], NM_001011645.3:c.*4735TA[28], NM_001011645.3:c.*4735TA[29], NM_001011645.3:c.*4735TA[30], NM_001011645.3:c.*4735TA[31], NM_001011645.3:c.*4735TA[32], NM_001011645.2:c.*4735TA[4], NM_001011645.2:c.*4735TA[5], NM_001011645.2:c.*4735TA[6], NM_001011645.2:c.*4735TA[7], NM_001011645.2:c.*4735TA[8], NM_001011645.2:c.*4735TA[9], NM_001011645.2:c.*4735TA[10], NM_001011645.2:c.*4735TA[11], NM_001011645.2:c.*4735TA[12], NM_001011645.2:c.*4735TA[13], NM_001011645.2:c.*4735TA[14], NM_001011645.2:c.*4735TA[15], NM_001011645.2:c.*4735TA[16], NM_001011645.2:c.*4735TA[17], NM_001011645.2:c.*4735TA[18], NM_001011645.2:c.*4735TA[19], NM_001011645.2:c.*4735TA[21], NM_001011645.2:c.*4735TA[22], NM_001011645.2:c.*4735TA[23], NM_001011645.2:c.*4735TA[24], NM_001011645.2:c.*4735TA[25], NM_001011645.2:c.*4735TA[26], NM_001011645.2:c.*4735TA[27], NM_001011645.2:c.*4735TA[28], NM_001011645.2:c.*4735TA[29], NM_001011645.2:c.*4735TA[30], NM_001011645.2:c.*4735TA[31], NM_001011645.2:c.*4735TA[32]

Select item 14914188805.

rs1491418880 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: X:67723354 (GRCh38)
X:66943196 (GRCh37)
Canonical SPDI:: NC_000023.11:67723353:CA:
Gene:: AR (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00068/11 (ALFA)
-=0.00187/166 (GnomAD)
-=0.00786/101 (TOMMO)
HGVS:: NC_000023.11:g.67723354_67723355del, NC_000023.10:g.66943196_66943197del, NG_009014.2:g.184323_184324del

Select item 14914045306.

rs1491404530 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AT [Show Flanks]
Chromosome:: X:67626608 (GRCh38)
X:66846451 (GRCh37)
Canonical SPDI:: NC_000023.11:67626608:T:TAT
Gene:: AR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TAT=0./0 (ALFA)
HGVS:: NC_000023.11:g.67626609_67626610insAT, NC_000023.10:g.66846451_66846452insAT, NG_009014.2:g.87578_87579insAT

Select item 14913944247.

rs1491394424 has merged into rs35442632 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: X:67577015 (GRCh38)
X:66796857 (GRCh37)
Canonical SPDI:: NC_000023.11:67577004:TTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000023.11:67577004:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000023.11:67577004:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000023.11:67577004:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000023.11:67577004:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000023.11:67577004:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000023.11:67577004:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000023.11:67577004:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000023.11:67577004:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67577004:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67577004:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67577004:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67577004:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67577004:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: AR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
-=0.14781/558 (1000Genomes)
HGVS:: NC_000023.11:g.67577015_67577021del, NC_000023.11:g.67577018_67577021del, NC_000023.11:g.67577019_67577021del, NC_000023.11:g.67577020_67577021del, NC_000023.11:g.67577021del, NC_000023.11:g.67577021dup, NC_000023.11:g.67577020_67577021dup, NC_000023.11:g.67577019_67577021dup, NC_000023.11:g.67577018_67577021dup, NC_000023.11:g.67577016_67577021dup, NC_000023.11:g.67577015_67577021dup, NC_000023.11:g.67577014_67577021dup, NC_000023.11:g.67577011_67577021dup, NC_000023.11:g.67577006_67577021dup, NC_000023.10:g.66796857_66796863del, NC_000023.10:g.66796860_66796863del, NC_000023.10:g.66796861_66796863del, NC_000023.10:g.66796862_66796863del, NC_000023.10:g.66796863del, NC_000023.10:g.66796863dup, NC_000023.10:g.66796862_66796863dup, NC_000023.10:g.66796861_66796863dup, NC_000023.10:g.66796860_66796863dup, NC_000023.10:g.66796858_66796863dup, NC_000023.10:g.66796857_66796863dup, NC_000023.10:g.66796856_66796863dup, NC_000023.10:g.66796853_66796863dup, NC_000023.10:g.66796848_66796863dup, NG_009014.2:g.37984_37990del, NG_009014.2:g.37987_37990del, NG_009014.2:g.37988_37990del, NG_009014.2:g.37989_37990del, NG_009014.2:g.37990del, NG_009014.2:g.37990dup, NG_009014.2:g.37989_37990dup, NG_009014.2:g.37988_37990dup, NG_009014.2:g.37987_37990dup, NG_009014.2:g.37985_37990dup, NG_009014.2:g.37984_37990dup, NG_009014.2:g.37983_37990dup, NG_009014.2:g.37980_37990dup, NG_009014.2:g.37975_37990dup

Select item 14913595728.

rs1491359572 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GT,GTGT,GTGTGT,GTGTGTGTGTGTGTGTGT [Show Flanks]
Chromosome:: X:67604196 (GRCh38)
X:66824039 (GRCh37)
Canonical SPDI:: NC_000023.11:67604196:T:TGT,NC_000023.11:67604196:T:TGTGT,NC_000023.11:67604196:T:TGTGTGT,NC_000023.11:67604196:T:TGTGTGTGTGTGTGTGTGT
Gene:: AR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGT=0./0 (ALFA)
TG=0.00027/3 (TOMMO)
HGVS:: NC_000023.11:g.67604197_67604198insGT, NC_000023.11:g.67604197_67604198insGTGT, NC_000023.11:g.67604198GT[3], NC_000023.11:g.67604198GT[9], NC_000023.10:g.66824039_66824040insGT, NC_000023.10:g.66824039_66824040insGTGT, NC_000023.10:g.66824040GT[3], NC_000023.10:g.66824040GT[9], NG_009014.2:g.65166_65167insGT, NG_009014.2:g.65166_65167insGTGT, NG_009014.2:g.65167GT[3], NG_009014.2:g.65167GT[9]

Select item 14913535579.

rs1491353557 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: X:67551002 (GRCh38)
X:66770845 (GRCh37)
Canonical SPDI:: NC_000023.11:67551002::G
Gene:: AR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000021/1 (GnomAD)
HGVS:: NC_000023.11:g.67551002_67551003insG, NC_000023.10:g.66770844_66770845insG, NG_009014.2:g.11971_11972insG

Select item 149131697010.

rs1491316970 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CCACACAC [Show Flanks]
Chromosome:: X:67723521 (GRCh38)
X:66943364 (GRCh37)
Canonical SPDI:: NC_000023.11:67723521:CACACAC:CACACACCCACACAC
Gene:: AR (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
HGVS:: NC_000023.11:g.67723522_67723528CA[3]CCCACACAC[1], NC_000023.10:g.66943364_66943370CA[3]CCCACACAC[1], NG_009014.2:g.184491_184497CA[3]CCCACACAC[1]

Select item 149131453711.

rs1491314537 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: X:67728575 (GRCh38)
X:66948418 (GRCh37)
Canonical SPDI:: NC_000023.11:67728575:T:TT
Gene:: AR (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
T=0.0007/3 (GnomAD)
HGVS:: NC_000023.11:g.67728576dup, NC_000023.10:g.66948418dup, NG_009014.2:g.189545dup, NM_000044.6:c.*4735dup, NM_000044.5:c.*4735dup, NM_000044.4:c.*4735dup, NM_000044.3:c.*4735dup, NM_001011645.3:c.*4735dup, NM_001011645.2:c.*4735dup

Select item 149130642912.

rs1491306429 has merged into rs749055716 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>-,GTGT,GTGTGT,GTGTGTGT,GTGTGTGTGT [Show Flanks]
Chromosome:: X:67619351 (GRCh38)
X:66839193 (GRCh37)
Canonical SPDI:: NC_000023.11:67619331:TGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT,NC_000023.11:67619331:TGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:67619331:TGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:67619331:TGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:67619331:TGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Gene:: AR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGTGTGTGTGTGTGTGTGTGTGT=0./0 (ALFA)
TGTGTG=0.000015/4 (TOPMED)
TG=0.125/6 (Vietnamese)
HGVS:: NC_000023.11:g.67619333GT[9], NC_000023.11:g.67619333GT[11], NC_000023.11:g.67619333GT[12], NC_000023.11:g.67619333GT[13], NC_000023.11:g.67619333GT[14], NC_000023.10:g.66839175GT[9], NC_000023.10:g.66839175GT[11], NC_000023.10:g.66839175GT[12], NC_000023.10:g.66839175GT[13], NC_000023.10:g.66839175GT[14], NG_009014.2:g.80302GT[9], NG_009014.2:g.80302GT[11], NG_009014.2:g.80302GT[12], NG_009014.2:g.80302GT[13], NG_009014.2:g.80302GT[14]

Select item 149126678713.

rs1491266787 has merged into rs1213943835 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: X:67551017 (GRCh38)
X:66770859 (GRCh37)
Canonical SPDI:: NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:67551001:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: AR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000023.11:g.67551017_67551024del, NC_000023.11:g.67551019_67551024del, NC_000023.11:g.67551020_67551024del, NC_000023.11:g.67551021_67551024del, NC_000023.11:g.67551022_67551024del, NC_000023.11:g.67551023_67551024del, NC_000023.11:g.67551024del, NC_000023.11:g.67551024dup, NC_000023.11:g.67551023_67551024dup, NC_000023.11:g.67551022_67551024dup, NC_000023.11:g.67551021_67551024dup, NC_000023.11:g.67551020_67551024dup, NC_000023.11:g.67551019_67551024dup, NC_000023.11:g.67551018_67551024dup, NC_000023.11:g.67551017_67551024dup, NC_000023.11:g.67551016_67551024dup, NC_000023.11:g.67551015_67551024dup, NC_000023.11:g.67551014_67551024dup, NC_000023.11:g.67551013_67551024dup, NC_000023.11:g.67551024_67551025insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.66770859_66770866del, NC_000023.10:g.66770861_66770866del, NC_000023.10:g.66770862_66770866del, NC_000023.10:g.66770863_66770866del, NC_000023.10:g.66770864_66770866del, NC_000023.10:g.66770865_66770866del, NC_000023.10:g.66770866del, NC_000023.10:g.66770866dup, NC_000023.10:g.66770865_66770866dup, NC_000023.10:g.66770864_66770866dup, NC_000023.10:g.66770863_66770866dup, NC_000023.10:g.66770862_66770866dup, NC_000023.10:g.66770861_66770866dup, NC_000023.10:g.66770860_66770866dup, NC_000023.10:g.66770859_66770866dup, NC_000023.10:g.66770858_66770866dup, NC_000023.10:g.66770857_66770866dup, NC_000023.10:g.66770856_66770866dup, NC_000023.10:g.66770855_66770866dup, NC_000023.10:g.66770866_66770867insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_009014.2:g.11986_11993del, NG_009014.2:g.11988_11993del, NG_009014.2:g.11989_11993del, NG_009014.2:g.11990_11993del, NG_009014.2:g.11991_11993del, NG_009014.2:g.11992_11993del, NG_009014.2:g.11993del, NG_009014.2:g.11993dup, NG_009014.2:g.11992_11993dup, NG_009014.2:g.11991_11993dup, NG_009014.2:g.11990_11993dup, NG_009014.2:g.11989_11993dup, NG_009014.2:g.11988_11993dup, NG_009014.2:g.11987_11993dup, NG_009014.2:g.11986_11993dup, NG_009014.2:g.11985_11993dup, NG_009014.2:g.11984_11993dup, NG_009014.2:g.11983_11993dup, NG_009014.2:g.11982_11993dup, NG_009014.2:g.11993_11994insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149120612114.

rs1491206121 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAGAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: X:67624905 (GRCh38)
X:66844748 (GRCh37)
Canonical SPDI:: NC_000023.11:67624905:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000023.11:67624905:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: AR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAC=0.00046/7 (TOMMO)
HGVS:: NC_000023.11:g.67624906_67624934A[46]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000023.11:g.67624906_67624934A[34]GAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000023.10:g.66844748_66844776A[46]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000023.10:g.66844748_66844776A[34]GAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_009014.2:g.85875_85903A[46]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_009014.2:g.85875_85903A[34]GAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]

Select item 149118117815.

rs1491181178 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,TTTT [Show Flanks]
Chromosome:: X:67626610 (GRCh38)
X:66846452 (GRCh37)
Canonical SPDI:: NC_000023.11:67626607:TTTT:TT,NC_000023.11:67626607:TTTT:TTTTTT
Gene:: AR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTT=0./0 (ALFA)
-=0.00086/10 (TOMMO)
HGVS:: NC_000023.11:g.67626610_67626611del, NC_000023.11:g.67626610_67626611dup, NC_000023.10:g.66846452_66846453del, NC_000023.10:g.66846452_66846453dup, NG_009014.2:g.87579_87580del, NG_009014.2:g.87579_87580dup

Select item 149116764816.

rs1491167648 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CG [Show Flanks]
Chromosome:: X:67619332 (GRCh38)
X:66839175 (GRCh37)
Canonical SPDI:: NC_000023.11:67619332:G:GCG
Gene:: AR (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000023.11:g.67619333_67619334insCG, NC_000023.10:g.66839175_66839176insCG, NG_009014.2:g.80302_80303insCG

Select item 149107252817.

rs1491072528 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ATTT [Show Flanks]
Chromosome:: X:67626634 (GRCh38)
X:66846477 (GRCh37)
Canonical SPDI:: NC_000023.11:67626634:T:TATTT
Gene:: AR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TATTT=0./0 (ALFA)
TATT=0.00002/2 (GnomAD)
HGVS:: NC_000023.11:g.67626635_67626636insATTT, NC_000023.10:g.66846477_66846478insATTT, NG_009014.2:g.87604_87605insATTT

Select item 149106738518.

rs1491067385 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>-,AA [Show Flanks]
Chromosome:: X:67672715 (GRCh38)
X:66892557 (GRCh37)
Canonical SPDI:: NC_000023.11:67672714:AAAA:AAA,NC_000023.11:67672714:AAAA:AAAAA
Gene:: AR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AAAAA=0./0 (ALFA)
-=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.67672718del, NC_000023.11:g.67672718dup, NC_000023.10:g.66892560del, NC_000023.10:g.66892560dup, NG_009014.2:g.133687del, NG_009014.2:g.133687dup

Select item 149101950819.

rs1491019508 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: X:67641873 (GRCh38)
X:66861715 (GRCh37)
Canonical SPDI:: NC_000023.11:67641871:TCT:T
Gene:: AR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
-=0.00002/2 (GnomAD)
HGVS:: NC_000023.11:g.67641873_67641874del, NC_000023.10:g.66861715_66861716del, NG_009014.2:g.102842_102843del

Select item 149097330120.

rs1490973301 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:67618109 (GRCh38)
X:66837951 (GRCh37)
Canonical SPDI:: NC_000023.11:67618108:C:G
Gene:: AR (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000023.11:g.67618109C>G, NC_000023.10:g.66837951C>G, NG_009014.2:g.79078C>G

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