SNP Links for Nucleotide (Select 519666809) - SNP

Warning: The NCBI web site requires JavaScript to function. more...

Links from Nucleotide

Items: 1 to 20 of 498

<< First< Prev

Page of 25

Next >Last >>

Select item 14858804301.

rs1485880430 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:5737321 (GRCh38)
Y:5605362 (GRCh37)
Canonical SPDI:: NC_000024.10:5737320:A:G
Gene:: PCDH11Y (Varview)
Functional Consequence:: coding_sequence_variant,genic_downstream_transcript_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.00002/1 (GnomAD_exomes)
HGVS:: NC_000024.10:g.5737321A>G, NC_000024.9:g.5605362A>G, NG_011652.1:g.742096A>G, NM_032973.2:c.3402A>G, NM_001395587.1:c.3126A>G, XM_017030079.2:c.3369A>G, XM_017030079.1:c.3369A>G, XM_017030080.2:c.3369A>G, XM_017030080.1:c.3369A>G, XM_017030081.2:c.3369A>G, XM_017030081.1:c.3369A>G

Select item 14858261532.

rs1485826153 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:5099782 (GRCh38)
Y:4967823 (GRCh37)
Canonical SPDI:: NC_000024.10:5099781:A:G
Gene:: PCDH11Y (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0.0004/2 (ALFA)
G=0.00003/2 (GnomAD_exomes)
HGVS:: NC_000024.10:g.5099782A>G, NC_000024.9:g.4967823A>G, NG_011652.1:g.104557A>G, NM_032972.3:c.2204A>G, NM_032972.2:c.2204A>G, NM_032971.3:c.2171A>G, NM_032971.2:c.2171A>G, NM_032973.2:c.2204A>G, NM_001278619.2:c.2171A>G, NM_001278619.1:c.2171A>G, NM_001395587.1:c.1928A>G, XM_017030079.2:c.2171A>G, XM_017030079.1:c.2171A>G, XM_017030080.2:c.2171A>G, XM_017030080.1:c.2171A>G, XM_017030081.2:c.2171A>G, XM_017030081.1:c.2171A>G, NP_116754.1:p.Asn735Ser, NP_116753.1:p.Asn724Ser, NP_116755.1:p.Asn735Ser, NP_001265548.1:p.Asn724Ser, NP_001382516.1:p.Asn643Ser, XP_016885568.1:p.Asn724Ser, XP_016885569.1:p.Asn724Ser, XP_016885570.1:p.Asn724Ser

Select item 14848485173.

rs1484848517 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:5098918 (GRCh38)
Y:4966959 (GRCh37)
Canonical SPDI:: NC_000024.10:5098917:A:G
Gene:: PCDH11Y (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.00001/1 (GnomAD_exomes)
HGVS:: NC_000024.10:g.5098918A>G, NC_000024.9:g.4966959A>G, NG_011652.1:g.103693A>G, NM_032972.3:c.1340A>G, NM_032972.2:c.1340A>G, NM_032971.3:c.1307A>G, NM_032971.2:c.1307A>G, NM_032973.2:c.1340A>G, NM_001278619.2:c.1307A>G, NM_001278619.1:c.1307A>G, NM_001395587.1:c.1064A>G, XM_017030079.2:c.1307A>G, XM_017030079.1:c.1307A>G, XM_017030080.2:c.1307A>G, XM_017030080.1:c.1307A>G, XM_017030081.2:c.1307A>G, XM_017030081.1:c.1307A>G, NP_116754.1:p.Gln447Arg, NP_116753.1:p.Gln436Arg, NP_116755.1:p.Gln447Arg, NP_001265548.1:p.Gln436Arg, NP_001382516.1:p.Gln355Arg, XP_016885568.1:p.Gln436Arg, XP_016885569.1:p.Gln436Arg, XP_016885570.1:p.Gln436Arg

Select item 14847159414.

rs1484715941 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:5099079 (GRCh38)
Y:4967120 (GRCh37)
Canonical SPDI:: NC_000024.10:5099078:T:C
Gene:: PCDH11Y (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.00001/1 (GnomAD_exomes)
HGVS:: NC_000024.10:g.5099079T>C, NC_000024.9:g.4967120T>C, NG_011652.1:g.103854T>C, NM_032972.3:c.1501T>C, NM_032972.2:c.1501T>C, NM_032971.3:c.1468T>C, NM_032971.2:c.1468T>C, NM_032973.2:c.1501T>C, NM_001278619.2:c.1468T>C, NM_001278619.1:c.1468T>C, NM_001395587.1:c.1225T>C, XM_017030079.2:c.1468T>C, XM_017030079.1:c.1468T>C, XM_017030080.2:c.1468T>C, XM_017030080.1:c.1468T>C, XM_017030081.2:c.1468T>C, XM_017030081.1:c.1468T>C, NP_116754.1:p.Ser501Pro, NP_116753.1:p.Ser490Pro, NP_116755.1:p.Ser501Pro, NP_001265548.1:p.Ser490Pro, NP_001382516.1:p.Ser409Pro, XP_016885568.1:p.Ser490Pro, XP_016885569.1:p.Ser490Pro, XP_016885570.1:p.Ser490Pro

Select item 14705296245.

rs1470529624 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:5100383 (GRCh38)
Y:4968424 (GRCh37)
Canonical SPDI:: NC_000024.10:5100382:C:T
Gene:: PCDH11Y (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000024.10:g.5100383C>T, NC_000024.9:g.4968424C>T, NG_011652.1:g.105158C>T, NM_032972.3:c.2805C>T, NM_032972.2:c.2805C>T, NM_032971.3:c.2772C>T, NM_032971.2:c.2772C>T, NM_032973.2:c.2805C>T, NM_001278619.2:c.2772C>T, NM_001278619.1:c.2772C>T, NM_001395587.1:c.2529C>T, XM_017030079.2:c.2772C>T, XM_017030079.1:c.2772C>T, XM_017030080.2:c.2772C>T, XM_017030080.1:c.2772C>T, XM_017030081.2:c.2772C>T, XM_017030081.1:c.2772C>T

Select item 14671645346.

rs1467164534 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: Y:5099625 (GRCh38)
Y:4967667 (GRCh37)
Canonical SPDI:: NC_000024.10:5099625:T:TT
Gene:: PCDH11Y (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.00002/1 (GnomAD_exomes)
HGVS:: NC_000024.10:g.5099626dup, NC_000024.9:g.4967667dup, NG_011652.1:g.104401dup, NM_032972.3:c.2048dup, NM_032972.2:c.2048dup, NM_032971.3:c.2015dup, NM_032971.2:c.2015dup, NM_032973.2:c.2048dup, NM_001278619.2:c.2015dup, NM_001278619.1:c.2015dup, NM_001395587.1:c.1772dup, XM_017030079.2:c.2015dup, XM_017030079.1:c.2015dup, XM_017030080.2:c.2015dup, XM_017030080.1:c.2015dup, XM_017030081.2:c.2015dup, XM_017030081.1:c.2015dup, NP_116754.1:p.Ser684fs, NP_116753.1:p.Ser673fs, NP_116755.1:p.Ser684fs, NP_001265548.1:p.Ser673fs, NP_001382516.1:p.Ser592fs, XP_016885568.1:p.Ser673fs, XP_016885569.1:p.Ser673fs, XP_016885570.1:p.Ser673fs

Select item 14656146847.

rs1465614684 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:5057066 (GRCh38)
Y:4925107 (GRCh37)
Canonical SPDI:: NC_000024.10:5057065:G:A
Gene:: PCDH11Y (Varview)
Functional Consequence:: coding_sequence_variant,5_prime_UTR_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.00013/9 (GnomAD_exomes)
HGVS:: NC_000024.10:g.5057066G>A, NC_000024.9:g.4925107G>A, NG_011652.1:g.61841G>A, NM_032972.3:c.243G>A, NM_032972.2:c.243G>A, NM_032971.3:c.210G>A, NM_032971.2:c.210G>A, NM_032973.2:c.243G>A, NM_001278619.2:c.210G>A, NM_001278619.1:c.210G>A, NM_001395587.1:c.-34G>A, XM_017030079.2:c.210G>A, XM_017030079.1:c.210G>A, XM_017030080.2:c.210G>A, XM_017030080.1:c.210G>A, XM_017030081.2:c.210G>A, XM_017030081.1:c.210G>A

Select item 14635118828.

rs1463511882 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: Y:5737749 (GRCh38)
Y:5605790 (GRCh37)
Canonical SPDI:: NC_000024.10:5737748:A:C
Gene:: PCDH11Y (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency
MAF:: C=0.00001/1 (GnomAD_exomes)
HGVS:: NC_000024.10:g.5737749A>C, NC_000024.9:g.5605790A>C, NG_011652.1:g.742524A>C, NM_032973.2:c.3830A>C, NM_001395587.1:c.3554A>C, XM_017030079.2:c.3797A>C, XM_017030079.1:c.3797A>C, XM_017030080.2:c.3797A>C, XM_017030080.1:c.3797A>C, XM_017030081.2:c.3797A>C, XM_017030081.1:c.3797A>C, NP_116755.1:p.Gln1277Pro, NP_001382516.1:p.Gln1185Pro, XP_016885568.1:p.Gln1266Pro, XP_016885569.1:p.Gln1266Pro, XP_016885570.1:p.Gln1266Pro

Select item 14615789819.

rs1461578981 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:5740944 (GRCh38)
Y:5608985 (GRCh37)
Canonical SPDI:: NC_000024.10:5740943:A:G
Gene:: PCDH11Y (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
HGVS:: NC_000024.10:g.5740944A>G, NC_000024.9:g.5608985A>G, NG_011652.1:g.745719A>G, NM_032973.2:c.*3002A>G, NM_001395587.1:c.*3002A>G, XM_017030079.2:c.*3002A>G, XM_017030079.1:c.*3002A>G, XM_017030080.2:c.*3002A>G, XM_017030080.1:c.*3002A>G, XM_017030081.2:c.*3002A>G, XM_017030081.1:c.*3002A>G

Select item 146040232710.

rs1460402327 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: Y:5099817 (GRCh38)
Y:4967858 (GRCh37)
Canonical SPDI:: NC_000024.10:5099816:A:T
Gene:: PCDH11Y (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.00001/1 (GnomAD_exomes)
HGVS:: NC_000024.10:g.5099817A>T, NC_000024.9:g.4967858A>T, NG_011652.1:g.104592A>T, NM_032972.3:c.2239A>T, NM_032972.2:c.2239A>T, NM_032971.3:c.2206A>T, NM_032971.2:c.2206A>T, NM_032973.2:c.2239A>T, NM_001278619.2:c.2206A>T, NM_001278619.1:c.2206A>T, NM_001395587.1:c.1963A>T, XM_017030079.2:c.2206A>T, XM_017030079.1:c.2206A>T, XM_017030080.2:c.2206A>T, XM_017030080.1:c.2206A>T, XM_017030081.2:c.2206A>T, XM_017030081.1:c.2206A>T, NP_116754.1:p.Ile747Phe, NP_116753.1:p.Ile736Phe, NP_116755.1:p.Ile747Phe, NP_001265548.1:p.Ile736Phe, NP_001382516.1:p.Ile655Phe, XP_016885568.1:p.Ile736Phe, XP_016885569.1:p.Ile736Phe, XP_016885570.1:p.Ile736Phe

Select item 145820916611.

rs1458209166 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTATCAC>- [Show Flanks]
Chromosome:: Y:5098597 (GRCh38)
Y:4966638 (GRCh37)
Canonical SPDI:: NC_000024.10:5098594:ACTTATCAC:AC
Gene:: PCDH11Y (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
HGVS:: NC_000024.10:g.5098597_5098603del, NC_000024.9:g.4966638_4966644del, NG_011652.1:g.103372_103378del, NM_032972.3:c.1019_1025del, NM_032972.2:c.1019_1025del, NM_032971.3:c.986_992del, NM_032971.2:c.986_992del, NM_032973.2:c.1019_1025del, NM_001278619.2:c.986_992del, NM_001278619.1:c.986_992del, NM_001395587.1:c.743_749del, XM_017030079.2:c.986_992del, XM_017030079.1:c.986_992del, XM_017030080.2:c.986_992del, XM_017030080.1:c.986_992del, XM_017030081.2:c.986_992del, XM_017030081.1:c.986_992del, NP_116754.1:p.Leu340fs, NP_116753.1:p.Leu329fs, NP_116755.1:p.Leu340fs, NP_001265548.1:p.Leu329fs, NP_001382516.1:p.Leu248fs, XP_016885568.1:p.Leu329fs, XP_016885569.1:p.Leu329fs, XP_016885570.1:p.Leu329fs

Select item 145402742512.

rs1454027425 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: Y:5737532 (GRCh38)
Y:5605573 (GRCh37)
Canonical SPDI:: NC_000024.10:5737531:C:A
Gene:: PCDH11Y (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency
MAF:: A=0.00001/1 (GnomAD_exomes)
HGVS:: NC_000024.10:g.5737532C>A, NC_000024.9:g.5605573C>A, NG_011652.1:g.742307C>A, NM_032973.2:c.3613C>A, NM_001395587.1:c.3337C>A, XM_017030079.2:c.3580C>A, XM_017030079.1:c.3580C>A, XM_017030080.2:c.3580C>A, XM_017030080.1:c.3580C>A, XM_017030081.2:c.3580C>A, XM_017030081.1:c.3580C>A, NP_116755.1:p.Pro1205Thr, NP_001382516.1:p.Pro1113Thr, XP_016885568.1:p.Pro1194Thr, XP_016885569.1:p.Pro1194Thr, XP_016885570.1:p.Pro1194Thr

Select item 145266859913.

rs1452668599 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:5099363 (GRCh38)
Y:4967404 (GRCh37)
Canonical SPDI:: NC_000024.10:5099362:G:A
Gene:: PCDH11Y (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.00003/2 (GnomAD_exomes)
HGVS:: NC_000024.10:g.5099363G>A, NC_000024.9:g.4967404G>A, NG_011652.1:g.104138G>A, NM_032972.3:c.1785G>A, NM_032972.2:c.1785G>A, NM_032971.3:c.1752G>A, NM_032971.2:c.1752G>A, NM_032973.2:c.1785G>A, NM_001278619.2:c.1752G>A, NM_001278619.1:c.1752G>A, NM_001395587.1:c.1509G>A, XM_017030079.2:c.1752G>A, XM_017030079.1:c.1752G>A, XM_017030080.2:c.1752G>A, XM_017030080.1:c.1752G>A, XM_017030081.2:c.1752G>A, XM_017030081.1:c.1752G>A

Select item 145203923014.

rs1452039230 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: Y:5099339 (GRCh38)
Y:4967380 (GRCh37)
Canonical SPDI:: NC_000024.10:5099338:A:
Gene:: PCDH11Y (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency
MAF:: -=0.00001/1 (GnomAD_exomes)
HGVS:: NC_000024.10:g.5099339del, NC_000024.9:g.4967380del, NG_011652.1:g.104114del, NM_032972.3:c.1761del, NM_032972.2:c.1761del, NM_032971.3:c.1728del, NM_032971.2:c.1728del, NM_032973.2:c.1761del, NM_001278619.2:c.1728del, NM_001278619.1:c.1728del, NM_001395587.1:c.1485del, XM_017030079.2:c.1728del, XM_017030079.1:c.1728del, XM_017030080.2:c.1728del, XM_017030080.1:c.1728del, XM_017030081.2:c.1728del, XM_017030081.1:c.1728del, NP_116754.1:p.Val588fs, NP_116753.1:p.Val577fs, NP_116755.1:p.Val588fs, NP_001265548.1:p.Val577fs, NP_001382516.1:p.Val496fs, XP_016885568.1:p.Val577fs, XP_016885569.1:p.Val577fs, XP_016885570.1:p.Val577fs

Select item 145034789115.

rs1450347891 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:5501133 (GRCh38)
Y:5369174 (GRCh37)
Canonical SPDI:: NC_000024.10:5501132:A:G
Gene:: PCDH11Y (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
HGVS:: NC_000024.10:g.5501133A>G, NC_000024.9:g.5369174A>G, NG_011652.1:g.505908A>G, NM_032973.2:c.3206A>G, NM_001395587.1:c.2930A>G, XM_017030079.2:c.3173A>G, XM_017030079.1:c.3173A>G, XM_017030080.2:c.3173A>G, XM_017030080.1:c.3173A>G, XM_017030081.2:c.3173A>G, XM_017030081.1:c.3173A>G, NP_116755.1:p.Asp1069Gly, NP_001382516.1:p.Asp977Gly, XP_016885568.1:p.Asp1058Gly, XP_016885569.1:p.Asp1058Gly, XP_016885570.1:p.Asp1058Gly

Select item 144757688416.

rs1447576884 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:5737513 (GRCh38)
Y:5605554 (GRCh37)
Canonical SPDI:: NC_000024.10:5737512:C:T
Gene:: PCDH11Y (Varview)
Functional Consequence:: coding_sequence_variant,genic_downstream_transcript_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.00003/2 (GnomAD_exomes)
HGVS:: NC_000024.10:g.5737513C>T, NC_000024.9:g.5605554C>T, NG_011652.1:g.742288C>T, NM_032973.2:c.3594C>T, NM_001395587.1:c.3318C>T, XM_017030079.2:c.3561C>T, XM_017030079.1:c.3561C>T, XM_017030080.2:c.3561C>T, XM_017030080.1:c.3561C>T, XM_017030081.2:c.3561C>T, XM_017030081.1:c.3561C>T

Select item 144679610617.

rs1446796106 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:5099085 (GRCh38)
Y:4967126 (GRCh37)
Canonical SPDI:: NC_000024.10:5099084:G:A
Gene:: PCDH11Y (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.0004/2 (ALFA)
A=0.00004/3 (GnomAD_exomes)
HGVS:: NC_000024.10:g.5099085G>A, NC_000024.9:g.4967126G>A, NG_011652.1:g.103860G>A, NM_032972.3:c.1507G>A, NM_032972.2:c.1507G>A, NM_032971.3:c.1474G>A, NM_032971.2:c.1474G>A, NM_032973.2:c.1507G>A, NM_001278619.2:c.1474G>A, NM_001278619.1:c.1474G>A, NM_001395587.1:c.1231G>A, XM_017030079.2:c.1474G>A, XM_017030079.1:c.1474G>A, XM_017030080.2:c.1474G>A, XM_017030080.1:c.1474G>A, XM_017030081.2:c.1474G>A, XM_017030081.1:c.1474G>A, NP_116754.1:p.Val503Ile, NP_116753.1:p.Val492Ile, NP_116755.1:p.Val503Ile, NP_001265548.1:p.Val492Ile, NP_001382516.1:p.Val411Ile, XP_016885568.1:p.Val492Ile, XP_016885569.1:p.Val492Ile, XP_016885570.1:p.Val492Ile

Select item 144421400018.

rs1444214000 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:5098872 (GRCh38)
Y:4966913 (GRCh37)
Canonical SPDI:: NC_000024.10:5098871:A:G
Gene:: PCDH11Y (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.00001/1 (GnomAD_exomes)
HGVS:: NC_000024.10:g.5098872A>G, NC_000024.9:g.4966913A>G, NG_011652.1:g.103647A>G, NM_032972.3:c.1294A>G, NM_032972.2:c.1294A>G, NM_032971.3:c.1261A>G, NM_032971.2:c.1261A>G, NM_032973.2:c.1294A>G, NM_001278619.2:c.1261A>G, NM_001278619.1:c.1261A>G, NM_001395587.1:c.1018A>G, XM_017030079.2:c.1261A>G, XM_017030079.1:c.1261A>G, XM_017030080.2:c.1261A>G, XM_017030080.1:c.1261A>G, XM_017030081.2:c.1261A>G, XM_017030081.1:c.1261A>G, NP_116754.1:p.Thr432Ala, NP_116753.1:p.Thr421Ala, NP_116755.1:p.Thr432Ala, NP_001265548.1:p.Thr421Ala, NP_001382516.1:p.Thr340Ala, XP_016885568.1:p.Thr421Ala, XP_016885569.1:p.Thr421Ala, XP_016885570.1:p.Thr421Ala

Select item 144153191719.

rs1441531917 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:5501084 (GRCh38)
Y:5369125 (GRCh37)
Canonical SPDI:: NC_000024.10:5501083:C:T
Gene:: PCDH11Y (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency
MAF:: T=0.00001/1 (GnomAD_exomes)
HGVS:: NC_000024.10:g.5501084C>T, NC_000024.9:g.5369125C>T, NG_011652.1:g.505859C>T, NM_032973.2:c.3157C>T, NM_001395587.1:c.2881C>T, XM_017030079.2:c.3124C>T, XM_017030079.1:c.3124C>T, XM_017030080.2:c.3124C>T, XM_017030080.1:c.3124C>T, XM_017030081.2:c.3124C>T, XM_017030081.1:c.3124C>T, NP_116755.1:p.Pro1053Ser, NP_001382516.1:p.Pro961Ser, XP_016885568.1:p.Pro1042Ser, XP_016885569.1:p.Pro1042Ser, XP_016885570.1:p.Pro1042Ser

Select item 143939306420.

rs1439393064 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: Y:5057379 (GRCh38)
Y:4925420 (GRCh37)
Canonical SPDI:: NC_000024.10:5057378:A:C
Gene:: PCDH11Y (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.00001/1 (GnomAD_exomes)
HGVS:: NC_000024.10:g.5057379A>C, NC_000024.9:g.4925420A>C, NG_011652.1:g.62154A>C, NM_032972.3:c.556A>C, NM_032972.2:c.556A>C, NM_032971.3:c.523A>C, NM_032971.2:c.523A>C, NM_032973.2:c.556A>C, NM_001278619.2:c.523A>C, NM_001278619.1:c.523A>C, NM_001395587.1:c.280A>C, XM_017030079.2:c.523A>C, XM_017030079.1:c.523A>C, XM_017030080.2:c.523A>C, XM_017030080.1:c.523A>C, XM_017030081.2:c.523A>C, XM_017030081.1:c.523A>C, NP_116754.1:p.Ile186Leu, NP_116753.1:p.Ile175Leu, NP_116755.1:p.Ile186Leu, NP_001265548.1:p.Ile175Leu, NP_001382516.1:p.Ile94Leu, XP_016885568.1:p.Ile175Leu, XP_016885569.1:p.Ile175Leu, XP_016885570.1:p.Ile175Leu

<< First< Prev

Page of 25

Next >Last >>

Supplemental Content

Filters: Manage Filters

Find related data

Recent activity

Clear Turn Off Turn On

SNP Links for Nucleotide (Select 519666809) (498)
SNP

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to: