SNP Links for Nucleotide (Select 1004170634) - SNP

Select item 14300614461.

rs1430061446 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:21880639 (GRCh38)
Y:24026786 (GRCh37)
Canonical SPDI:: NC_000024.10:21880638:A:G
Gene:: RBMY1D (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
HGVS:: NC_000024.10:g.21880639A>G, NC_000024.9:g.24026786A>G, NG_004755.2:g.69753A>G, NM_001006120.3:c.1206T>C, NM_001006120.2:c.1206T>C, XM_011531486.2:c.1206T>C, XM_011531486.1:c.1206T>C, XM_011531489.2:c.873T>C, XM_011531489.1:c.873T>C, NM_001320950.1:c.1023T>C, NM_001320949.1:c.1095T>C, XM_047442737.1:c.786T>C

Select item 13458332072.

rs1345833207 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:21880633 (GRCh38)
Y:24026780 (GRCh37)
Canonical SPDI:: NC_000024.10:21880632:T:C
Gene:: RBMY1D (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
HGVS:: NC_000024.10:g.21880633T>C, NC_000024.9:g.24026780T>C, NG_004755.2:g.69747T>C, NM_001006120.3:c.1212A>G, NM_001006120.2:c.1212A>G, XM_011531486.2:c.1212A>G, XM_011531486.1:c.1212A>G, XM_011531489.2:c.879A>G, XM_011531489.1:c.879A>G, NM_001320950.1:c.1029A>G, NM_001320949.1:c.1101A>G, XM_047442737.1:c.792A>G

Select item 12873628443.

rs1287362844 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: Y:21880645 (GRCh38)
Y:24026792 (GRCh37)
Canonical SPDI:: NC_000024.10:21880644:A:T
Gene:: RBMY1D (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
HGVS:: NC_000024.10:g.21880645A>T, NC_000024.9:g.24026792A>T, NG_004755.2:g.69759A>T, NM_001006120.3:c.1200T>A, NM_001006120.2:c.1200T>A, XM_011531486.2:c.1200T>A, XM_011531486.1:c.1200T>A, XM_011531489.2:c.867T>A, XM_011531489.1:c.867T>A, NM_001320950.1:c.1017T>A, NM_001320949.1:c.1089T>A, XM_047442737.1:c.780T>A

Select item 8792107104.

rs879210710 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: Y:21880565 (GRCh38)
Y:24026712 (GRCh37)
Canonical SPDI:: NC_000024.10:21880564:C:G
Gene:: RBMY1D (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
HGVS:: NC_000024.10:g.21880565C>G, NC_000024.9:g.24026712C>G, NG_004755.2:g.69679C>G, NM_001006120.3:c.1280G>C, NM_001006120.2:c.1280G>C, XM_011531486.2:c.1280G>C, XM_011531486.1:c.1280G>C, XM_011531489.2:c.947G>C, XM_011531489.1:c.947G>C, NM_001320950.1:c.1097G>C, NM_001320949.1:c.1169G>C, XM_047442737.1:c.860G>C, NP_001006120.2:p.Arg427Thr, XP_011529788.1:p.Arg427Thr, XP_011529791.1:p.Arg316Thr, NP_001307879.1:p.Arg366Thr, NP_001307878.1:p.Arg390Thr, XP_047298693.1:p.Arg287Thr

Select item 7961519585.

rs796151958 [Homo sapiens]

dbSNP