65147560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101276481-G-A

65147560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101276481-G-T

65147674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101276576-T-C

65147674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101276576-T-G

http://identifiers.org/hco/1/GRCh38#65147755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101276590-C-A

65147755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101276590-C-G

65147755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101276590-C-T

65147758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101276593-G-T

65147793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101276617-G-A

65147793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101276617-G-C

65147793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101276617-G-T

http://identifiers.org/hco/1/GRCh38#65147806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101276630-A-C

65147806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101276630-A-G

65147806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101276630-A-T

65147850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101276666-G-T

65147880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101276696-G-C

65147880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101276696-G-T

65147912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101276714-G-A

65147912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101276714-G-T

65148088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101276779-T-A

65148088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101276779-T-C

http://identifiers.org/hco/1/GRCh38#65148149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101276823-A-C

65148149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101276823-A-G

65148149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101276823-A-T

65148155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101276852-A-G

65148155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101276852-A-T

65148157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101276854-G-A

65148157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101276854-G-T

http://identifiers.org/hco/1/GRCh38#65148162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101276859-C-A

65148162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101276859-C-G

65148162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101276859-C-T

65148170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101276867-T-A

65148170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101276867-T-C

65148170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101276867-T-G

65148258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101276906-G-C

65148558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277168-G-A

65148558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277168-G-T

65148562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277178-T-C

65148710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277351-G-T

65148872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277494-T-A

65148872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277494-T-C

65148872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277494-T-G

http://identifiers.org/hco/1/GRCh38#65148874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101277496-C-A

65148874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277496-C-T

65148877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277499-T-A

65148877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277499-T-C

http://identifiers.org/hco/1/GRCh38#65148908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101277525-A-C

http://identifiers.org/hco/1/GRCh38#65148967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101277570-A-C

65148967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277570-A-G

65148967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277570-A-T

65149025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101277609-T-A

65149025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101277609-T-C

65149025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101277609-T-G

http://identifiers.org/hco/1/GRCh38#65149158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101277738-A-C

65149158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277738-A-G

http://identifiers.org/hco/1/GRCh38#65149159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101277739-C-A

65149159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277739-C-T

http://identifiers.org/hco/1/GRCh38#65149172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101277752-C-A

65149172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277752-C-G

65149172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277752-C-T

http://identifiers.org/hco/1/GRCh38#65149181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101277761-C-A

65149181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277761-C-G

65149181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277761-C-T

65149400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277931-C-G

65149723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101278218-C-T

65149741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101278236-G-T

65149742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101278237-C-G

65149742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101278237-C-T

65150642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101280031-C-T

65151472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101280654-C-T

65151475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101280657-G-T

65151551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101280718-C-T

65151575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101280745-A-G

65152191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101281723-T-A

65158811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101285156-C-T

65159152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101285485-G-A

65161190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101287180-T-C

65161368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101287352-T-C

65161376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101287360-C-G

65161403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101287387-G-C

65161403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101287387-G-T

65161404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101287388-C-T

65161415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101287403-G-A

http://identifiers.org/hco/1/GRCh38#65167392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101289467-A-C

65167736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101289804-C-T

65170553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101294463-A-G

65170784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101294802-T-C

65172307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101295612-G-A

http://identifiers.org/hco/1/GRCh38#65172313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101295618-A-C

65172313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101295618-A-G

65172666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101295958-G-A

65175390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101297016-A-T

65175455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101297077-C-T

65175642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101297213-G-A

65175712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101297275-A-T

65175855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101297404-A-G

65180367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101297929-T-G

65180486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101298030-A-G

65180764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101300005-C-T

65180809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101300039-C-T

65180926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101300148-G-A

65181020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101300222-T-G

65181154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101300429-T-A

65181154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101300429-T-G

65181212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101300480-G-A

65181244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101300524-T-C

65181314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101300587-A-G

65183790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101301612-G-C

65184664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101302081-G-A

65185007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101302368-C-T

65185069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101302409-T-A

65190809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101304456-G-A

http://identifiers.org/hco/1/GRCh38#65190855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101304500-A-C

http://identifiers.org/hco/1/GRCh38#65190885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101304516-C-A

65190932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101304564-A-G

65191092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101304684-C-T

65191127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101304722-G-A

65191233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101304814-T-C

65195694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101307301-T-A

65195761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101307358-A-G

65195988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101307550-C-T

65196017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101307594-T-A

65196308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101307891-G-A

http://identifiers.org/hco/1/GRCh38#65196584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101308104-C-A

65197662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101309994-G-A

65197698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101310029-A-G

http://identifiers.org/hco/1/GRCh38#65197703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101310034-C-A

65198456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101310436-C-T

65198622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101310659-T-G

65198664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101310718-A-G

65198769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101310809-C-T

65198770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101310810-A-T

65208293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101314350-T-C

65208333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101314379-C-T

65208372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101314413-G-A

65208792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101314761-A-G

65208970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101314883-C-T

65209004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101314911-A-T

65209015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101314918-C-T

http://identifiers.org/hco/1/GRCh38#65209493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101315747-C-A

65209513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101315764-G-A

65218218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101317379-C-T

65218307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101317463-T-C

65218519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101317614-C-G

65218716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101317661-A-G

65218773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101317716-A-G

65218866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101317809-T-C

65218884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101317827-C-T

65221651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101318983-A-G

65221789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101319094-T-C

65221820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101319123-C-T

65222746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101319360-C-G

65222844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101319412-G-C

65222952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101319511-G-C

65222968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101319526-G-A

65223036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101319653-T-A

65224637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101320041-A-T

65224683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101320082-A-G

65224725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101320120-A-G

http://identifiers.org/hco/1/GRCh38#65224908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101320305-C-A

65224908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101320305-C-T

65224927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101320310-G-A

65224981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101320346-A-G

65224983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101320348-T-A

65224983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101320348-T-C

65225022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101320378-G-A

65226017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101320710-G-A

65226017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101320710-G-T

65226026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101320719-C-G

65226212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101320898-A-G

65226212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101320898-A-T

65226225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101320911-T-C

65226225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101320911-T-G

65226226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101320912-G-A

65226365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101321057-A-G

http://identifiers.org/hco/1/GRCh38#65226400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101321066-C-A

65226400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101321066-C-T

http://identifiers.org/hco/1/GRCh38#65226459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101321123-A-C

65226914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101321460-A-G

65226914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101321460-A-T

65226950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101321498-G-T

65226968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101321520-C-T

65227199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101321708-A-G

65227235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101321744-G-T

65227821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101322293-G-A

65227841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101322312-C-T

65227915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101322383-A-G

65227957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101322412-G-T

http://identifiers.org/hco/1/GRCh38#65227970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101322425-C-A

65228080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101322514-A-G

65228083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101322517-G-T

65228109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101322543-T-G

65228712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101322927-T-C

65228789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101322963-G-T

65228820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101322990-T-C

65228972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101323099-A-G

65228978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101323105-C-T

65228988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101323115-A-G

65229160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101323262-A-G

65229211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101323311-A-G

65231178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 101323481-A-G

65231225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101323512-A-G

http://identifiers.org/hco/1/GRCh38#65231246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#101323532-C-A

65231522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101323752-C-T

65231804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 101323918-G-T

65231938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 101324003-A-G

65231940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 101324005-G-T

65231942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 101324007-G-A

65231960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101324021-G-A

65231960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101324021-G-T

65231973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101324032-C-T

65231977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101324036-C-T

65231993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101324052-G-A

65231995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101324054-A-G

http://identifiers.org/hco/1/GRCh38#65232016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101324064-C-A

65232016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 363
most severe consequence: 3 prime UTR variant
orthologous variants: 101324064-C-T