SNP Links for Protein (Select 68448544) - SNP

Select item 14879830381.

rs1487983038 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:150407252 (GRCh38)
5:149786815 (GRCh37)
Canonical SPDI:: NC_000005.10:150407251:G:A
Gene:: CD74 (Varview)
Functional Consequence:: synonymous_variant,non_coding_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000005.10:g.150407252G>A, NC_000005.9:g.149786815G>A, NG_029730.1:g.10685C>T, NM_004355.4:c.198C>T, NM_004355.3:c.198C>T, NM_001025159.3:c.198C>T, NM_001025159.2:c.198C>T, NR_157074.3:n.359C>T, NR_157074.2:n.205C>T, NR_157074.1:n.205C>T, NM_001364083.3:c.198C>T, NM_001364083.2:c.198C>T, NM_001364083.1:c.198C>T, NM_001364084.3:c.198C>T, NM_001364084.2:c.198C>T, NM_001364084.1:c.198C>T, NM_001025158.3:c.198C>T, NM_001025158.2:c.198C>T

Select item 14859771932.

rs1485977193 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:150406938 (GRCh38)
5:149786501 (GRCh37)
Canonical SPDI:: NC_000005.10:150406937:C:T
Gene:: CD74 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
HGVS:: NC_000005.10:g.150406938C>T, NC_000005.9:g.149786501C>T, NG_029730.1:g.10999G>A, NM_004355.4:c.321G>A, NM_004355.3:c.321G>A, NM_001025159.3:c.321G>A, NM_001025159.2:c.321G>A, NR_157074.3:n.482G>A, NR_157074.2:n.328G>A, NR_157074.1:n.328G>A, NM_001364083.3:c.321G>A, NM_001364083.2:c.321G>A, NM_001364083.1:c.321G>A, NM_001364084.3:c.321G>A, NM_001364084.2:c.321G>A, NM_001364084.1:c.321G>A, NM_001025158.3:c.321G>A, NM_001025158.2:c.321G>A, NP_004346.1:p.Met107Ile, NP_001020330.1:p.Met107Ile, NP_001351012.1:p.Met107Ile, NP_001351013.1:p.Met107Ile, NP_001020329.1:p.Met107Ile

Select item 14853284693.

rs1485328469 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 5:150404691 (GRCh38)
5:149784254 (GRCh37)
Canonical SPDI:: NC_000005.10:150404690:G:A,NC_000005.10:150404690:G:C
Gene:: CD74 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.150404691G>A, NC_000005.10:g.150404691G>C, NC_000005.9:g.149784254G>A, NC_000005.9:g.149784254G>C, NG_029730.1:g.13246C>T, NG_029730.1:g.13246C>G, NM_004355.4:c.614C>T, NM_004355.4:c.614C>G, NM_004355.3:c.614C>T, NM_004355.3:c.614C>G, NM_001025159.3:c.614C>T, NM_001025159.3:c.614C>G, NM_001025159.2:c.614C>T, NM_001025159.2:c.614C>G, NM_001364083.3:c.551C>T, NM_001364083.3:c.551C>G, NM_001364083.2:c.551C>T, NM_001364083.2:c.551C>G, NM_001364083.1:c.551C>T, NM_001364083.1:c.551C>G, NP_004346.1:p.Ala205Val, NP_004346.1:p.Ala205Gly, NP_001020330.1:p.Ala205Val, NP_001020330.1:p.Ala205Gly, NP_001351012.1:p.Ala184Val, NP_001351012.1:p.Ala184Gly

Select item 14791311304.

rs1479131130 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 5:150402601 (GRCh38)
5:149782164 (GRCh37)
Canonical SPDI:: NC_000005.10:150402600:G:A,NC_000005.10:150402600:G:C,NC_000005.10:150402600:G:T
Gene:: CD74 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.150402601G>A, NC_000005.10:g.150402601G>C, NC_000005.10:g.150402601G>T, NC_000005.9:g.149782164G>A, NC_000005.9:g.149782164G>C, NC_000005.9:g.149782164G>T, NG_029730.1:g.15336C>T, NG_029730.1:g.15336C>G, NG_029730.1:g.15336C>A, NM_004355.4:c.650C>T, NM_004355.4:c.650C>G, NM_004355.4:c.650C>A, NM_004355.3:c.650C>T, NM_004355.3:c.650C>G, NM_004355.3:c.650C>A, NM_001025159.3:c.842C>T, NM_001025159.3:c.842C>G, NM_001025159.3:c.842C>A, NM_001025159.2:c.842C>T, NM_001025159.2:c.842C>G, NM_001025159.2:c.842C>A, NR_157074.3:n.819C>T, NR_157074.3:n.819C>G, NR_157074.3:n.819C>A, NR_157074.2:n.665C>T, NR_157074.2:n.665C>G, NR_157074.2:n.665C>A, NR_157074.1:n.665C>T, NR_157074.1:n.665C>G, NR_157074.1:n.665C>A, NM_001364083.3:c.587C>T, NM_001364083.3:c.587C>G, NM_001364083.3:c.587C>A, NM_001364083.2:c.587C>T, NM_001364083.2:c.587C>G, NM_001364083.2:c.587C>A, NM_001364083.1:c.587C>T, NM_001364083.1:c.587C>G, NM_001364083.1:c.587C>A, NM_001364084.3:c.562C>T, NM_001364084.3:c.562C>G, NM_001364084.3:c.562C>A, NM_001364084.2:c.562C>T, NM_001364084.2:c.562C>G, NM_001364084.2:c.562C>A, NM_001364084.1:c.562C>T, NM_001364084.1:c.562C>G, NM_001364084.1:c.562C>A, NM_001025158.3:c.466C>T, NM_001025158.3:c.466C>G, NM_001025158.3:c.466C>A, NM_001025158.2:c.466C>T, NM_001025158.2:c.466C>G, NM_001025158.2:c.466C>A, NP_004346.1:p.Ser217Phe, NP_004346.1:p.Ser217Cys, NP_004346.1:p.Ser217Tyr, NP_001020330.1:p.Ser281Phe, NP_001020330.1:p.Ser281Cys, NP_001020330.1:p.Ser281Tyr, NP_001351012.1:p.Ser196Phe, NP_001351012.1:p.Ser196Cys, NP_001351012.1:p.Ser196Tyr, NP_001351013.1:p.Leu188Phe, NP_001351013.1:p.Leu188Val, NP_001351013.1:p.Leu188Ile, NP_001020329.1:p.Leu156Phe, NP_001020329.1:p.Leu156Val, NP_001020329.1:p.Leu156Ile

Select item 14759369305.

rs1475936930 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 5:150403187 (GRCh38)
5:149782750 (GRCh37)
Canonical SPDI:: NC_000005.10:150403186:A:G,NC_000005.10:150403186:A:T
Gene:: CD74 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
G=0.000035/1 (TOMMO)
HGVS:: NC_000005.10:g.150403187A>G, NC_000005.10:g.150403187A>T, NC_000005.9:g.149782750A>G, NC_000005.9:g.149782750A>T, NG_029730.1:g.14750T>C, NG_029730.1:g.14750T>A, NM_001025159.3:c.751T>C, NM_001025159.3:c.751T>A, NM_001025159.2:c.751T>C, NM_001025159.2:c.751T>A, NR_157074.3:n.728T>C, NR_157074.3:n.728T>A, NR_157074.2:n.574T>C, NR_157074.2:n.574T>A, NR_157074.1:n.574T>C, NR_157074.1:n.574T>A, NP_001020330.1:p.Trp251Arg, NP_001020330.1:p.Trp251Arg

Select item 14745690916.

rs1474569091 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:150405164 (GRCh38)
5:149784727 (GRCh37)
Canonical SPDI:: NC_000005.10:150405163:T:C
Gene:: CD74 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
HGVS:: NC_000005.10:g.150405164T>C, NC_000005.9:g.149784727T>C, NG_029730.1:g.12773A>G, NM_004355.4:c.458A>G, NM_004355.3:c.458A>G, NM_001025159.3:c.458A>G, NM_001025159.2:c.458A>G, NM_001364083.3:c.395A>G, NM_001364083.2:c.395A>G, NM_001364083.1:c.395A>G, NM_001364084.3:c.458A>G, NM_001364084.2:c.458A>G, NM_001364084.1:c.458A>G, NP_004346.1:p.Lys153Arg, NP_001020330.1:p.Lys153Arg, NP_001351012.1:p.Lys132Arg, NP_001351013.1:p.Lys153Arg

Select item 14739425717.

rs1473942571 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 5:150412700 (GRCh38)
5:149792263 (GRCh37)
Canonical SPDI:: NC_000005.10:150412699:A:G
Gene:: CD74 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (GnomAD_exomes)
G=0.000011/3 (TOPMED)
HGVS:: NC_000005.10:g.150412700A>G, NC_000005.9:g.149792263A>G, NG_029730.1:g.5237T>C, NM_004355.4:c.50T>C, NM_004355.3:c.50T>C, NM_001025159.3:c.50T>C, NM_001025159.2:c.50T>C, NR_157074.3:n.211T>C, NR_157074.2:n.57T>C, NR_157074.1:n.57T>C, NM_001364083.3:c.50T>C, NM_001364083.2:c.50T>C, NM_001364083.1:c.50T>C, NM_001364084.3:c.50T>C, NM_001364084.2:c.50T>C, NM_001364084.1:c.50T>C, NM_001025158.3:c.50T>C, NM_001025158.2:c.50T>C, NP_004346.1:p.Met17Thr, NP_001020330.1:p.Met17Thr, NP_001351012.1:p.Met17Thr, NP_001351013.1:p.Met17Thr, NP_001020329.1:p.Met17Thr

Select item 14658428728.

rs1465842872 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 5:150403204 (GRCh38)
5:149782767 (GRCh37)
Canonical SPDI:: NC_000005.10:150403203:C:A,NC_000005.10:150403203:C:G,NC_000005.10:150403203:C:T
Gene:: CD74 (Varview)
Functional Consequence:: missense_variant,non_coding_transcript_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000005.10:g.150403204C>A, NC_000005.10:g.150403204C>G, NC_000005.10:g.150403204C>T, NC_000005.9:g.149782767C>A, NC_000005.9:g.149782767C>G, NC_000005.9:g.149782767C>T, NG_029730.1:g.14733G>T, NG_029730.1:g.14733G>C, NG_029730.1:g.14733G>A, NM_001025159.3:c.734G>T, NM_001025159.3:c.734G>C, NM_001025159.3:c.734G>A, NM_001025159.2:c.734G>T, NM_001025159.2:c.734G>C, NM_001025159.2:c.734G>A, NR_157074.3:n.711G>T, NR_157074.3:n.711G>C, NR_157074.3:n.711G>A, NR_157074.2:n.557G>T, NR_157074.2:n.557G>C, NR_157074.2:n.557G>A, NR_157074.1:n.557G>T, NR_157074.1:n.557G>C, NR_157074.1:n.557G>A, NP_001020330.1:p.Gly245Val, NP_001020330.1:p.Gly245Ala, NP_001020330.1:p.Gly245Glu

Select item 14626654079.

rs1462665407 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 5:150403121 (GRCh38)
5:149782684 (GRCh37)
Canonical SPDI:: NC_000005.10:150403120:C:A,NC_000005.10:150403120:C:G,NC_000005.10:150403120:C:T
Gene:: CD74 (Varview)
Functional Consequence:: missense_variant,non_coding_transcript_variant,stop_gained,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.150403121C>A, NC_000005.10:g.150403121C>G, NC_000005.10:g.150403121C>T, NC_000005.9:g.149782684C>A, NC_000005.9:g.149782684C>G, NC_000005.9:g.149782684C>T, NG_029730.1:g.14816G>T, NG_029730.1:g.14816G>C, NG_029730.1:g.14816G>A, NM_001025159.3:c.817G>T, NM_001025159.3:c.817G>C, NM_001025159.3:c.817G>A, NM_001025159.2:c.817G>T, NM_001025159.2:c.817G>C, NM_001025159.2:c.817G>A, NR_157074.3:n.794G>T, NR_157074.3:n.794G>C, NR_157074.3:n.794G>A, NR_157074.2:n.640G>T, NR_157074.2:n.640G>C, NR_157074.2:n.640G>A, NR_157074.1:n.640G>T, NR_157074.1:n.640G>C, NR_157074.1:n.640G>A, NP_001020330.1:p.Glu273Ter, NP_001020330.1:p.Glu273Gln, NP_001020330.1:p.Glu273Lys

Select item 146213143910.

rs1462131439 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:150404731 (GRCh38)
5:149784294 (GRCh37)
Canonical SPDI:: NC_000005.10:150404730:C:T
Gene:: CD74 (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0.000111/1 (ALFA)
T=0.00001/2 (GnomAD_exomes)
HGVS:: NC_000005.10:g.150404731C>T, NC_000005.9:g.149784294C>T, NG_029730.1:g.13206G>A, NM_004355.4:c.574G>A, NM_004355.3:c.574G>A, NM_001025159.3:c.574G>A, NM_001025159.2:c.574G>A, NM_001364083.3:c.511G>A, NM_001364083.2:c.511G>A, NM_001364083.1:c.511G>A, NP_004346.1:p.Glu192Lys, NP_001020330.1:p.Glu192Lys, NP_001351012.1:p.Glu171Lys

Select item 146184618911.

rs1461846189 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 5:150403281 (GRCh38)
5:149782844 (GRCh37)
Canonical SPDI:: NC_000005.10:150403280:G:A,NC_000005.10:150403280:G:C
Gene:: CD74 (Varview)
Functional Consequence:: missense_variant,non_coding_transcript_variant,synonymous_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.150403281G>A, NC_000005.10:g.150403281G>C, NC_000005.9:g.149782844G>A, NC_000005.9:g.149782844G>C, NG_029730.1:g.14656C>T, NG_029730.1:g.14656C>G, NM_001025159.3:c.657C>T, NM_001025159.3:c.657C>G, NM_001025159.2:c.657C>T, NM_001025159.2:c.657C>G, NR_157074.3:n.634C>T, NR_157074.3:n.634C>G, NR_157074.2:n.480C>T, NR_157074.2:n.480C>G, NR_157074.1:n.480C>T, NR_157074.1:n.480C>G, NP_001020330.1:p.His219Gln

Select item 145632493212.

rs1456324932 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:150407158 (GRCh38)
5:149786721 (GRCh37)
Canonical SPDI:: NC_000005.10:150407157:G:A
Gene:: CD74 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000005.10:g.150407158G>A, NC_000005.9:g.149786721G>A, NG_029730.1:g.10779C>T, NM_004355.4:c.292C>T, NM_004355.3:c.292C>T, NM_001025159.3:c.292C>T, NM_001025159.2:c.292C>T, NR_157074.3:n.453C>T, NR_157074.2:n.299C>T, NR_157074.1:n.299C>T, NM_001364083.3:c.292C>T, NM_001364083.2:c.292C>T, NM_001364083.1:c.292C>T, NM_001364084.3:c.292C>T, NM_001364084.2:c.292C>T, NM_001364084.1:c.292C>T, NM_001025158.3:c.292C>T, NM_001025158.2:c.292C>T, NP_004346.1:p.Pro98Ser, NP_001020330.1:p.Pro98Ser, NP_001351012.1:p.Pro98Ser, NP_001351013.1:p.Pro98Ser, NP_001020329.1:p.Pro98Ser

Select item 145536139213.

rs1455361392 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:150412643 (GRCh38)
5:149792206 (GRCh37)
Canonical SPDI:: NC_000005.10:150412642:C:T
Gene:: CD74 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000005.10:g.150412643C>T, NC_000005.9:g.149792206C>T, NG_029730.1:g.5294G>A, NM_004355.4:c.107G>A, NM_004355.3:c.107G>A, NM_001025159.3:c.107G>A, NM_001025159.2:c.107G>A, NR_157074.3:n.268G>A, NR_157074.2:n.114G>A, NR_157074.1:n.114G>A, NM_001364083.3:c.107G>A, NM_001364083.2:c.107G>A, NM_001364083.1:c.107G>A, NM_001364084.3:c.107G>A, NM_001364084.2:c.107G>A, NM_001364084.1:c.107G>A, NM_001025158.3:c.107G>A, NM_001025158.2:c.107G>A, NP_004346.1:p.Arg36His, NP_001020330.1:p.Arg36His, NP_001351012.1:p.Arg36His, NP_001351013.1:p.Arg36His, NP_001020329.1:p.Arg36His

Select item 145404222014.

rs1454042220 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 5:150406917 (GRCh38)
5:149786480 (GRCh37)
Canonical SPDI:: NC_000005.10:150406916:C:A,NC_000005.10:150406916:C:T
Gene:: CD74 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000248/4 (TOMMO)
HGVS:: NC_000005.10:g.150406917C>A, NC_000005.10:g.150406917C>T, NC_000005.9:g.149786480C>A, NC_000005.9:g.149786480C>T, NG_029730.1:g.11020G>T, NG_029730.1:g.11020G>A, NM_004355.4:c.342G>T, NM_004355.4:c.342G>A, NM_004355.3:c.342G>T, NM_004355.3:c.342G>A, NM_001025159.3:c.342G>T, NM_001025159.3:c.342G>A, NM_001025159.2:c.342G>T, NM_001025159.2:c.342G>A, NR_157074.3:n.503G>T, NR_157074.3:n.503G>A, NR_157074.2:n.349G>T, NR_157074.2:n.349G>A, NR_157074.1:n.349G>T, NR_157074.1:n.349G>A, NM_001364083.3:c.342G>T, NM_001364083.3:c.342G>A, NM_001364083.2:c.342G>T, NM_001364083.2:c.342G>A, NM_001364083.1:c.342G>T, NM_001364083.1:c.342G>A, NM_001364084.3:c.342G>T, NM_001364084.3:c.342G>A, NM_001364084.2:c.342G>T, NM_001364084.2:c.342G>A, NM_001364084.1:c.342G>T, NM_001364084.1:c.342G>A, NM_001025158.3:c.342G>T, NM_001025158.3:c.342G>A, NM_001025158.2:c.342G>T, NM_001025158.2:c.342G>A

Select item 145303064715.

rs1453030647 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 5:150404697 (GRCh38)
5:149784260 (GRCh37)
Canonical SPDI:: NC_000005.10:150404696:G:A,NC_000005.10:150404696:G:C,NC_000005.10:150404696:G:T
Gene:: CD74 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000005.10:g.150404697G>A, NC_000005.10:g.150404697G>C, NC_000005.10:g.150404697G>T, NC_000005.9:g.149784260G>A, NC_000005.9:g.149784260G>C, NC_000005.9:g.149784260G>T, NG_029730.1:g.13240C>T, NG_029730.1:g.13240C>G, NG_029730.1:g.13240C>A, NM_004355.4:c.608C>T, NM_004355.4:c.608C>G, NM_004355.4:c.608C>A, NM_004355.3:c.608C>T, NM_004355.3:c.608C>G, NM_004355.3:c.608C>A, NM_001025159.3:c.608C>T, NM_001025159.3:c.608C>G, NM_001025159.3:c.608C>A, NM_001025159.2:c.608C>T, NM_001025159.2:c.608C>G, NM_001025159.2:c.608C>A, NM_001364083.3:c.545C>T, NM_001364083.3:c.545C>G, NM_001364083.3:c.545C>A, NM_001364083.2:c.545C>T, NM_001364083.2:c.545C>G, NM_001364083.2:c.545C>A, NM_001364083.1:c.545C>T, NM_001364083.1:c.545C>G, NM_001364083.1:c.545C>A, NP_004346.1:p.Thr203Ile, NP_004346.1:p.Thr203Ser, NP_004346.1:p.Thr203Asn, NP_001020330.1:p.Thr203Ile, NP_001020330.1:p.Thr203Ser, NP_001020330.1:p.Thr203Asn, NP_001351012.1:p.Thr182Ile, NP_001351012.1:p.Thr182Ser, NP_001351012.1:p.Thr182Asn

Select item 145094109116.

rs1450941091 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 5:150406304 (GRCh38)
5:149785867 (GRCh37)
Canonical SPDI:: NC_000005.10:150406303:G:A,NC_000005.10:150406303:G:C
Gene:: CD74 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000051/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000005.10:g.150406304G>A, NC_000005.10:g.150406304G>C, NC_000005.9:g.149785867G>A, NC_000005.9:g.149785867G>C, NG_029730.1:g.11633C>T, NG_029730.1:g.11633C>G, NM_004355.4:c.396C>T, NM_004355.4:c.396C>G, NM_004355.3:c.396C>T, NM_004355.3:c.396C>G, NM_001025159.3:c.396C>T, NM_001025159.3:c.396C>G, NM_001025159.2:c.396C>T, NM_001025159.2:c.396C>G, NR_157074.3:n.557C>T, NR_157074.3:n.557C>G, NR_157074.2:n.403C>T, NR_157074.2:n.403C>G, NR_157074.1:n.403C>T, NR_157074.1:n.403C>G, NM_001364084.3:c.396C>T, NM_001364084.3:c.396C>G, NM_001364084.2:c.396C>T, NM_001364084.2:c.396C>G, NM_001364084.1:c.396C>T, NM_001364084.1:c.396C>G, NM_001025158.3:c.396C>T, NM_001025158.3:c.396C>G, NM_001025158.2:c.396C>T, NM_001025158.2:c.396C>G

Select item 144682407917.

rs1446824079 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 5:150405126 (GRCh38)
5:149784689 (GRCh37)
Canonical SPDI:: NC_000005.10:150405125:G:A,NC_000005.10:150405125:G:T
Gene:: CD74 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000045/12 (TOPMED)
HGVS:: NC_000005.10:g.150405126G>A, NC_000005.10:g.150405126G>T, NC_000005.9:g.149784689G>A, NC_000005.9:g.149784689G>T, NG_029730.1:g.12811C>T, NG_029730.1:g.12811C>A, NM_004355.4:c.496C>T, NM_004355.4:c.496C>A, NM_004355.3:c.496C>T, NM_004355.3:c.496C>A, NM_001025159.3:c.496C>T, NM_001025159.3:c.496C>A, NM_001025159.2:c.496C>T, NM_001025159.2:c.496C>A, NM_001364083.3:c.433C>T, NM_001364083.3:c.433C>A, NM_001364083.2:c.433C>T, NM_001364083.2:c.433C>A, NM_001364083.1:c.433C>T, NM_001364083.1:c.433C>A, NM_001364084.3:c.496C>T, NM_001364084.3:c.496C>A, NM_001364084.2:c.496C>T, NM_001364084.2:c.496C>A, NM_001364084.1:c.496C>T, NM_001364084.1:c.496C>A, NP_004346.1:p.Leu166Met, NP_001020330.1:p.Leu166Met, NP_001351012.1:p.Leu145Met, NP_001351013.1:p.Leu166Met

Select item 144267801118.

rs1442678011 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 5:150402624 (GRCh38)
5:149782187 (GRCh37)
Canonical SPDI:: NC_000005.10:150402623:C:G,NC_000005.10:150402623:C:T
Gene:: CD74 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.150402624C>G, NC_000005.10:g.150402624C>T, NC_000005.9:g.149782187C>G, NC_000005.9:g.149782187C>T, NG_029730.1:g.15313G>C, NG_029730.1:g.15313G>A, NM_004355.4:c.627G>C, NM_004355.4:c.627G>A, NM_004355.3:c.627G>C, NM_004355.3:c.627G>A, NM_001025159.3:c.819G>C, NM_001025159.3:c.819G>A, NM_001025159.2:c.819G>C, NM_001025159.2:c.819G>A, NR_157074.3:n.796G>C, NR_157074.3:n.796G>A, NR_157074.2:n.642G>C, NR_157074.2:n.642G>A, NR_157074.1:n.642G>C, NR_157074.1:n.642G>A, NM_001364083.3:c.564G>C, NM_001364083.3:c.564G>A, NM_001364083.2:c.564G>C, NM_001364083.2:c.564G>A, NM_001364083.1:c.564G>C, NM_001364083.1:c.564G>A, NM_001364084.3:c.539G>C, NM_001364084.3:c.539G>A, NM_001364084.2:c.539G>C, NM_001364084.2:c.539G>A, NM_001364084.1:c.539G>C, NM_001364084.1:c.539G>A, NM_001025158.3:c.443G>C, NM_001025158.3:c.443G>A, NM_001025158.2:c.443G>C, NM_001025158.2:c.443G>A, NP_004346.1:p.Glu209Asp, NP_001020330.1:p.Glu273Asp, NP_001351012.1:p.Glu188Asp, NP_001351013.1:p.Ser180Thr, NP_001351013.1:p.Ser180Asn, NP_001020329.1:p.Ser148Thr, NP_001020329.1:p.Ser148Asn

Select item 144233930419.

rs1442339304 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:150406883 (GRCh38)
5:149786446 (GRCh37)
Canonical SPDI:: NC_000005.10:150406882:C:T
Gene:: CD74 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.150406883C>T, NC_000005.9:g.149786446C>T, NG_029730.1:g.11054G>A, NM_004355.4:c.376G>A, NM_004355.3:c.376G>A, NM_001025159.3:c.376G>A, NM_001025159.2:c.376G>A, NR_157074.3:n.537G>A, NR_157074.2:n.383G>A, NR_157074.1:n.383G>A, NM_001364083.3:c.376G>A, NM_001364083.2:c.376G>A, NM_001364083.1:c.376G>A, NM_001364084.3:c.376G>A, NM_001364084.2:c.376G>A, NM_001364084.1:c.376G>A, NM_001025158.3:c.376G>A, NM_001025158.2:c.376G>A, NP_004346.1:p.Gly126Arg, NP_001020330.1:p.Gly126Arg, NP_001351012.1:p.Gly126Arg, NP_001351013.1:p.Gly126Arg, NP_001020329.1:p.Gly126Arg

Select item 143929352220.

rs1439293522 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 5:150407179 (GRCh38)
5:149786742 (GRCh37)
Canonical SPDI:: NC_000005.10:150407178:C:G,NC_000005.10:150407178:C:T
Gene:: CD74 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000108/2 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000446/2 (Estonian)
HGVS:: NC_000005.10:g.150407179C>G, NC_000005.10:g.150407179C>T, NC_000005.9:g.149786742C>G, NC_000005.9:g.149786742C>T, NG_029730.1:g.10758G>C, NG_029730.1:g.10758G>A, NM_004355.4:c.271G>C, NM_004355.4:c.271G>A, NM_004355.3:c.271G>C, NM_004355.3:c.271G>A, NM_001025159.3:c.271G>C, NM_001025159.3:c.271G>A, NM_001025159.2:c.271G>C, NM_001025159.2:c.271G>A, NR_157074.3:n.432G>C, NR_157074.3:n.432G>A, NR_157074.2:n.278G>C, NR_157074.2:n.278G>A, NR_157074.1:n.278G>C, NR_157074.1:n.278G>A, NM_001364083.3:c.271G>C, NM_001364083.3:c.271G>A, NM_001364083.2:c.271G>C, NM_001364083.2:c.271G>A, NM_001364083.1:c.271G>C, NM_001364083.1:c.271G>A, NM_001364084.3:c.271G>C, NM_001364084.3:c.271G>A, NM_001364084.2:c.271G>C, NM_001364084.2:c.271G>A, NM_001364084.1:c.271G>C, NM_001364084.1:c.271G>A, NM_001025158.3:c.271G>C, NM_001025158.3:c.271G>A, NM_001025158.2:c.271G>C, NM_001025158.2:c.271G>A, NP_004346.1:p.Glu91Gln, NP_004346.1:p.Glu91Lys, NP_001020330.1:p.Glu91Gln, NP_001020330.1:p.Glu91Lys, NP_001351012.1:p.Glu91Gln, NP_001351012.1:p.Glu91Lys, NP_001351013.1:p.Glu91Gln, NP_001351013.1:p.Glu91Lys, NP_001020329.1:p.Glu91Gln, NP_001020329.1:p.Glu91Lys

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Result Filters

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Publication

Function Class

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Annotation

Global MAF

Custom range

Additional filters

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Items: 1 to 20 of 286

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