966510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 5 prime UTR variant
orthologous variants: 156312982-G-A

966510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 5 prime UTR variant
orthologous variants: 156312982-G-C

966746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156312729-G-T

966771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense_variant, undefined
orthologous variants: 156312704-G-A

966771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense_variant, undefined
orthologous variants: 156312704-G-T

http://identifiers.org/hco/1/GRCh38#966776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#156312699-C-A

966776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: synonymous_variant, undefined
orthologous variants: 156312699-C-T

966807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156312668-A-G

http://identifiers.org/hco/1/GRCh38#966818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#156312654-C-A

966818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, undefined
orthologous variants: 156312654-C-G

966818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, undefined
orthologous variants: 156312654-C-T

966832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, undefined
orthologous variants: 156312637-T-C

966849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, undefined
orthologous variants: 156312595-G-A

966849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, undefined
orthologous variants: 156312595-G-C

966849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, undefined
orthologous variants: 156312595-G-T

http://identifiers.org/hco/1/GRCh38#966852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#156312592-C-A

966852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, undefined
orthologous variants: 156312592-C-G

966852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, undefined
orthologous variants: 156312592-C-T

http://identifiers.org/hco/1/GRCh38#966877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156312541-C-A

966877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156312541-C-T

http://identifiers.org/hco/1/GRCh38#966883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156312535-A-C

966883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156312535-A-G

966904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156312512-G-T

966939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156312480-T-G

966971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, undefined
orthologous variants: 156312456-G-A

966971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, undefined
orthologous variants: 156312456-G-C

967048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156312383-C-T

967049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156312382-G-A

967050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156312381-G-C

967227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156312241-G-A

967271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, undefined
orthologous variants: 156312221-G-A

967283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156312209-C-T

967479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156312072-G-C

967542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156311996-C-T

967571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156311966-G-A

967638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156311917-A-T

967734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156311812-G-A

967734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156311812-G-T

968010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156311559-C-T

968099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156311468-G-A

968316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156311256-G-A

http://identifiers.org/hco/1/GRCh38#968464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156311161-C-A

968464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156311161-C-T

968489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156311136-T-C

968544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156311093-G-T

968616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156311022-G-A

968868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310825-C-T

969007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310655-G-A

969023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310639-C-T

969129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310533-C-G

969201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310447-G-A

969293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310357-C-T

969319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310327-G-A

969331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310312-G-A

969384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310262-C-T

http://identifiers.org/hco/1/GRCh38#970157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156310240-A-C

970157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310240-A-G

970160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310237-T-C

970173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310224-T-C

970177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310220-C-G

970222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310178-G-A

970222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310178-G-C

970231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310169-G-A

970231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310169-G-T

http://identifiers.org/hco/1/GRCh38#970240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156310160-A-C

970262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310141-C-G

970262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156310141-C-T

970298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: stop gained
orthologous variants: 156310106-C-T

970405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: synonymous variant
orthologous variants: 156309999-G-A

970405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: synonymous variant
orthologous variants: 156309999-G-T

970433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156309971-G-A

970433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156309971-G-C

970442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156309961-G-A

970448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156309955-C-T

970472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156309935-A-G

970472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156309935-A-T

970496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156309907-A-G

970584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156309820-G-A

970587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156309817-G-A

970594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156309810-C-T

970607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156309789-G-T

970641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156309768-T-C

970646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156309763-C-G

970646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156309763-C-T

970721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: synonymous variant
orthologous variants: 156309687-G-A

970721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: synonymous variant
orthologous variants: 156309687-G-C

970860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, missense_variant
orthologous variants: 156309524-C-G

970860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, missense_variant
orthologous variants: 156309524-C-T

970974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156309404-G-A

970974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156309404-G-C

970974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156309404-G-T

http://identifiers.org/hco/1/GRCh38#971003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156309375-A-C

971003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156309375-A-G

http://identifiers.org/hco/1/GRCh38#971015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156309363-C-A

971015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156309363-C-G

971015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156309363-C-T

http://identifiers.org/hco/1/GRCh38#971036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156309341-C-A

971046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156309331-C-T

http://identifiers.org/hco/1/GRCh38#971064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156309314-C-A

971077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 156309293-G-A

971077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 156309293-G-T

971159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156309229-G-A

971159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156309229-G-T

http://identifiers.org/hco/1/GRCh38#971194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156309194-C-A

971194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156309194-C-T

http://identifiers.org/hco/1/GRCh38#971269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156309140-C-A

971269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156309140-C-T

971271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156309138-G-A

971271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156309138-G-T

http://identifiers.org/hco/1/GRCh38#971283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156309126-C-A

http://identifiers.org/hco/1/GRCh38#971292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156309113-C-A

971292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156309113-C-T

971298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156309107-G-A

971298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156309107-G-T

http://identifiers.org/hco/1/GRCh38#971311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156309094-C-A

971311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156309094-C-G

971311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156309094-C-T

971436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156308964-G-C

971436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156308964-G-T

971460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156308940-A-G

971513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156308894-G-A

971513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156308894-G-C

971513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156308894-G-T

971564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308842-T-C

971573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308830-G-A

971573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308830-G-T

http://identifiers.org/hco/1/GRCh38#971577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156308826-C-A

971577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308826-C-T

http://identifiers.org/hco/1/GRCh38#971587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156308818-C-A

971587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308818-C-T

971588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308817-C-T

971590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308815-T-A

971590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308815-T-C

971672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308735-T-C

971750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308646-G-T

971780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308626-G-A

971865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308570-G-A

972098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 156308364-C-T

972164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308300-C-T

972201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308261-G-A

972214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308248-G-A

972215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308247-G-A

972215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308247-G-T

972308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 156308149-C-T

972338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 156308119-G-A

972338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 156308119-G-C

972338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 156308119-G-T

http://identifiers.org/hco/1/GRCh38#972370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156308087-C-A

http://identifiers.org/hco/1/GRCh38#972392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156308065-C-A

972406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: synonymous variant
orthologous variants: 156308051-G-A

972406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156308051-G-T

972416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156308041-G-A

972416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156308041-G-T

972473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308017-A-G

972532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156308007-G-C

972709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307980-T-C

972802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307947-G-A

972802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307947-G-T

972811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307938-G-A

972811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307938-G-T

972823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307926-G-A

972823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307926-G-C

972823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307926-G-T

972826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307923-C-T

972846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307910-T-A

972846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307910-T-C

http://identifiers.org/hco/1/GRCh38#972854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156307900-C-A

972854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 156307900-C-T

972859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, splice_acceptor_variant
orthologous variants: 156307895-A-G

972859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, splice_acceptor_variant
orthologous variants: 156307895-A-T

http://identifiers.org/hco/1/GRCh38#972876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156307878-C-A

972876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, stop_gained
orthologous variants: 156307878-C-T

http://identifiers.org/hco/1/GRCh38#972900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156307854-C-A

972900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156307854-C-G

972900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: stop_gained, synonymous_variant
orthologous variants: 156307854-C-T

http://identifiers.org/hco/1/GRCh38#972945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156307818-A-C

972969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 156307794-T-A

972969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 156307794-T-C

973039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307709-G-T

973040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307708-T-C

973041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307707-G-A

973041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307707-G-T

973042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307706-G-A

973042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307706-G-C

973042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307706-G-T

http://identifiers.org/hco/1/GRCh38#973088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156307662-C-A

973088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307662-C-T

973091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307632-G-A

973091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307632-G-T

973092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307631-G-A

973092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307631-G-T

973118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307605-G-T

http://identifiers.org/hco/1/GRCh38#973120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156307603-A-C

973130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307591-A-G

http://identifiers.org/hco/1/GRCh38#973148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156307573-C-A

http://identifiers.org/hco/1/GRCh38#973152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156307570-A-C

973153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307569-G-A

973239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 156307489-A-G

973291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 156307437-G-A

973291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 156307437-G-T

http://identifiers.org/hco/1/GRCh38#973294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156307434-C-A

973294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 156307434-C-G

973294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 156307434-C-T

http://identifiers.org/hco/1/GRCh38#973299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156307429-C-A

973299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 156307429-C-G

973299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 156307429-C-T

http://identifiers.org/hco/1/GRCh38#973303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156307425-C-A

973303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 156307425-C-G

973303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 156307425-C-T

973308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 156307414-G-A

973308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 156307414-G-C

http://identifiers.org/hco/1/GRCh38#973333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156307389-C-A

973333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 156307389-C-T

http://identifiers.org/hco/1/GRCh38#973392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156307336-C-A

973454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307280-G-A

973454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307280-G-C

973454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307280-G-T

973552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 156307183-A-G

973621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, missense_variant
orthologous variants: 156307114-A-G

973634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 156307101-G-A

973645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307090-G-A

http://identifiers.org/hco/1/GRCh38#973713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156307058-C-A

973713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307058-C-T

http://identifiers.org/hco/1/GRCh38#973741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156307030-C-A

973741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307030-C-G

973741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156307030-C-T

973799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306975-G-A

973799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306975-G-T

http://identifiers.org/hco/1/GRCh38#973843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156306923-C-A

973843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156306923-C-T

http://identifiers.org/hco/1/GRCh38#973885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156306881-C-A

973885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156306881-C-G

973885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156306881-C-T

973890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156306876-G-A

973890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156306876-G-T

973921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156306845-G-A

973921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156306845-G-T

http://identifiers.org/hco/1/GRCh38#973925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156306841-C-A

973925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: synonymous variant
orthologous variants: 156306841-C-T

973926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156306840-T-C

http://identifiers.org/hco/1/GRCh38#973933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156306833-C-A

973935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156306831-G-A

973935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156306831-G-T

973936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156306830-G-A

973936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156306830-G-T

973978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156306779-A-G

974083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306677-G-A

974083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306677-G-T

974104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306658-T-C

http://identifiers.org/hco/1/GRCh38#974142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156306628-A-C

974142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306628-A-G

http://identifiers.org/hco/1/GRCh38#974149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156306621-C-A

974149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306621-C-T

http://identifiers.org/hco/1/GRCh38#974173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156306596-C-A

974173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306596-C-T

http://identifiers.org/hco/1/GRCh38#974175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156306594-A-C

974175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306594-A-G

974175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306594-A-T

974204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306568-G-T

974216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306556-G-A

974216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306556-G-C

974223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306549-G-A

974223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306549-G-C

974237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306533-G-A

974286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306502-G-A

974286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306502-G-T

http://identifiers.org/hco/1/GRCh38#974300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156306488-C-A

974300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306488-C-T

974334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: missense variant
orthologous variants: 156306453-G-A

974370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306417-T-G

974373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306414-G-A

974392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306394-G-A

974399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306387-T-C

974407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306379-C-G

974407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306379-C-T

974416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron variant
orthologous variants: 156306370-T-G

974435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 156306344-C-T

974584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3 prime UTR variant
orthologous variants: 156306221-G-A

974584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3 prime UTR variant
orthologous variants: 156306221-G-C

974584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3 prime UTR variant
orthologous variants: 156306221-G-T

974601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156306204-G-A

974601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156306204-G-T

http://identifiers.org/hco/1/GRCh38#974610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156306185-C-A

974610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156306185-C-G

974610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156306185-C-T

974615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156306180-A-G

http://identifiers.org/hco/1/GRCh38#974631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156306158-C-A

974631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156306158-C-T

http://identifiers.org/hco/1/GRCh38#974642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156306144-C-A

974679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156306111-A-G

974679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156306111-A-T

974720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156306074-T-A

974720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156306074-T-C

http://identifiers.org/hco/1/GRCh38#974747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156306057-C-A

974747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156306057-C-G

974747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156306057-C-T

974764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156306039-G-A

974764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156306039-G-T

974806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156306013-G-T

http://identifiers.org/hco/1/GRCh38#974831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156305992-C-A

974831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305992-C-G

974831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305992-C-T

http://identifiers.org/hco/1/GRCh38#974853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156305980-C-A

http://identifiers.org/hco/1/GRCh38#974855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156305978-C-A

http://identifiers.org/hco/1/GRCh38#974870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156305964-C-A

http://identifiers.org/hco/1/GRCh38#974885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156305951-C-A

974885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305951-C-T

974891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305946-G-A

974891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305946-G-T

974906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305940-G-A

974906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305940-G-T

974913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305933-A-G

974927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305919-G-A

974927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305919-G-T

974930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305916-A-G

http://identifiers.org/hco/1/GRCh38#974939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156305903-C-A

974939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305903-C-T

974952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305891-T-C

974972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305871-G-A

974972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305871-G-T

975024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305833-G-A

975024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305833-G-T

http://identifiers.org/hco/1/GRCh38#975025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156305832-A-C

975025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305832-A-G

975025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305832-A-T

975036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305817-G-A

975036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305817-G-C

975036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305817-G-T

975047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305806-G-A

975047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305806-G-T

975054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305799-G-A

975054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 156305799-G-T

http://identifiers.org/hco/1/GRCh38#975087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156305767-C-A

975254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156305719-G-A

975254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156305719-G-T

975290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156305683-G-A

975290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156305683-G-T

http://identifiers.org/hco/1/GRCh38#975345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156305615-C-A

975345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156305615-C-T

http://identifiers.org/hco/1/GRCh38#975351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156305586-C-A

975351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156305586-C-T

975547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156305244-G-C

975578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156305212-G-A

975581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156305209-G-C

975616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156305187-G-A

975616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156305187-G-T

http://identifiers.org/hco/1/GRCh38#975627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156305175-C-A

975627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156305175-C-T

975659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156305138-T-C

http://identifiers.org/hco/1/GRCh38#975671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156305125-C-A

http://identifiers.org/hco/1/GRCh38#975683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156305113-C-A

975683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156305113-C-G

975683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156305113-C-T

http://identifiers.org/hco/1/GRCh38#975696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156305100-C-A

975696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156305100-C-T

http://identifiers.org/hco/1/GRCh38#975704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156305088-C-A

975746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156305057-T-C

975753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156305053-T-C

975753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156305053-T-G

975757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156305049-A-G

975757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156305049-A-T

975758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156305048-G-C

975864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25284
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156304969-T-C