225486779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181723900-G-A

225487166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181724271-C-T

225487299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181724397-G-A

http://identifiers.org/hco/1/GRCh38#225487341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181724437-C-A

225487341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181724437-C-T

225487347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181724443-C-T

http://identifiers.org/hco/1/GRCh38#225487370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181724461-C-A

225487370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181724461-C-T

http://identifiers.org/hco/1/GRCh38#225487380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181724469-A-C

225487380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181724469-A-G

225487405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181724494-T-C

225487490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181724564-C-G

225487610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181724670-A-G

225487690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181724743-C-T

225487766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181724824-T-C

225487766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181724824-T-G

http://identifiers.org/hco/1/GRCh38#225487841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181724893-C-A

225487841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181724893-C-T

225487849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181724901-A-G

http://identifiers.org/hco/1/GRCh38#225487892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181724934-C-A

225487993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181725013-T-C

http://identifiers.org/hco/1/GRCh38#225488052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181725072-C-A

http://identifiers.org/hco/1/GRCh38#225488312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181725256-C-A

225488322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181725266-T-C

http://identifiers.org/hco/1/GRCh38#225488367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181725311-C-A

225488399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181725324-G-C

225488453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181725375-A-G

225488562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181725448-G-A

225488562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181725448-G-T

225488686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181725558-C-T

225488770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181725645-T-G

225491935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181727670-A-T

225492036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181727734-A-G

http://identifiers.org/hco/1/GRCh38#225492041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181727739-A-C

225492055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181727750-T-C

225492069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181727765-T-G

225492072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181727768-A-T

225492448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181727876-A-G

225492456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181727884-A-G

225492506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181727923-C-T

225492672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181728071-G-A

225492748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181728122-T-C

http://identifiers.org/hco/1/GRCh38#225492766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181728142-C-A

225492767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181728143-A-G

http://identifiers.org/hco/1/GRCh38#225492794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181728170-C-A

225492798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181728174-A-G

225493244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181728863-C-G

225493277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181728906-G-A

225493277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181728906-G-T

225493532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181729108-T-C

225493625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181729194-G-A

http://identifiers.org/hco/1/GRCh38#225493642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181729211-A-C

225493642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181729211-A-G

225493666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181729231-T-C

225493787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181729472-A-G

http://identifiers.org/hco/1/GRCh38#225493799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181729484-C-A

225493829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181729513-T-A

225493936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181729597-G-A

225494198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181729815-G-T

http://identifiers.org/hco/1/GRCh38#225494202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181729819-C-A

http://identifiers.org/hco/1/GRCh38#225494220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181729837-C-A

225494222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181729839-A-T

225494312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181730048-G-T

225494921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181730615-G-A

225495116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181730793-C-T

225495297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181730962-A-G

225495427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181731073-G-A

225495427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3 prime UTR variant
orthologous variants: 181731073-G-T

225495985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181731619-C-T

225495986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181731620-G-A

225496055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181731686-G-T

http://identifiers.org/hco/1/GRCh38#225496130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181731768-C-A

http://identifiers.org/hco/1/GRCh38#225496153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181731791-C-A

225496238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181731884-G-T

225496273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181731971-G-A

225496279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181731977-G-A

225496279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181731977-G-T

225496301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181731999-G-C

225496301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181731999-G-T

http://identifiers.org/hco/1/GRCh38#225496349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181732041-C-A

225496349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181732041-C-T

225496485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181732179-G-T

http://identifiers.org/hco/1/GRCh38#225496789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181732488-A-C

http://identifiers.org/hco/1/GRCh38#225497383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181733064-A-C

http://identifiers.org/hco/1/GRCh38#225497546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181733211-C-A

225497546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181733211-C-T

225497661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181733321-T-A

225497746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181733396-A-G

http://identifiers.org/hco/1/GRCh38#225497830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181733481-A-C

225497890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181733539-T-C

225497932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181733581-T-A

225497932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181733581-T-C

225497932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181733581-T-G

http://identifiers.org/hco/1/GRCh38#225497953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181733601-A-C

225497953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181733601-A-G

225498211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181733853-T-C

http://identifiers.org/hco/1/GRCh38#225498218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181733857-A-C

225498218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181733857-A-G

http://identifiers.org/hco/1/GRCh38#225498299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181733908-A-C

225498325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181733931-G-A

225498325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181733931-G-C

225498484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181734103-T-C

225498484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181734103-T-G

225500580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181735459-T-C

225500872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181735742-A-G

225500872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181735742-A-T

http://identifiers.org/hco/1/GRCh38#225500882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181735757-C-A

225500908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181735782-G-A

225500908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181735782-G-T

225500945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181735798-A-T

http://identifiers.org/hco/1/GRCh38#225500955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181735821-A-C

225500977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181735848-C-T

225501043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181735914-G-C

225501043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181735914-G-T

225501150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181736021-A-T

http://identifiers.org/hco/1/GRCh38#225501194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181736061-C-A

225501308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181736177-C-T

225501312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181736181-T-C

225501394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181736257-G-T

http://identifiers.org/hco/1/GRCh38#225501806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181736644-C-A

225501931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181736771-G-C

225502073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181736884-G-A

225502077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181736891-T-A

225502077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181736891-T-G

http://identifiers.org/hco/1/GRCh38#225502625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181737097-A-C

225503856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181737920-C-T

225503901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181737969-A-T

http://identifiers.org/hco/1/GRCh38#225503992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181738042-C-A

http://identifiers.org/hco/1/GRCh38#225504053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181738099-C-A

225504053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181738099-C-T

225504216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181738346-C-T

225504439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181738537-T-C

225504449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181738547-T-C

225504601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181738802-T-A

225504602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181738803-T-A

http://identifiers.org/hco/1/GRCh38#225504893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181739061-C-A

225504893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181739061-C-T

225505123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181739294-G-A

225505123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181739294-G-C

225505123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181739294-G-T

225505454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181739611-T-A

225507381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181740379-A-G

225507637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181740613-C-T

225507824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181740775-G-A

225507923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181740844-T-C

225507931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181740852-T-C

225508038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181740959-A-G

225508052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181740976-T-C

225508177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181741085-A-G

225508335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181741383-T-C

225508691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181741895-G-C

225508726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181741933-C-T

225508875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181742087-A-G

225509457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181742614-G-A

225511686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181744653-A-G

http://identifiers.org/hco/1/GRCh38#225511713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181744684-C-A

http://identifiers.org/hco/1/GRCh38#225511958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181744913-C-A

225511958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181744913-C-T

225511977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181744928-T-A

225511977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181744928-T-C

225512032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181744967-T-C

225512051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181744985-C-G

225512521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181745669-A-G

225512587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181745740-A-G

http://identifiers.org/hco/1/GRCh38#225512658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181745824-C-A

225513034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181746168-G-A

225513034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181746168-G-C

225513034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181746168-G-T

225513157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181746275-T-C

225513179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181746299-A-G

http://identifiers.org/hco/1/GRCh38#225514491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181746791-A-C

225514491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181746791-A-G

225514695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181746989-A-G

225514695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181746989-A-T

225514716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181747010-T-G

225514755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181747049-G-A

225514755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181747049-G-C

225514755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181747049-G-T

http://identifiers.org/hco/1/GRCh38#225514761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181747055-A-C

225514761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181747055-A-G

225514761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181747055-A-T

http://identifiers.org/hco/1/GRCh38#225514767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181747061-C-A

225514767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181747061-C-G

225514767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181747061-C-T

http://identifiers.org/hco/1/GRCh38#225514776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181747073-C-A

225514776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181747073-C-G

225514776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181747073-C-T

225514785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181747082-T-C

225514785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181747082-T-G

225514844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 181747138-C-T

225514872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181747166-T-G

225514962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 181747255-T-G

http://identifiers.org/hco/1/GRCh38#225515068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181747364-C-A

225515068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 181747364-C-T

http://identifiers.org/hco/1/GRCh38#225515225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181747488-C-A

225515225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 181747488-C-T

225515231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 181747494-T-A

225515231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 181747494-T-C

225515257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 181747534-G-A

225515257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 181747534-G-T

225515258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 181747535-G-A

225515258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 181747535-G-T

225515339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 181747593-G-T

225515353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 181747607-A-T

http://identifiers.org/hco/1/GRCh38#225515454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181747684-C-A

225515454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181747684-C-T

http://identifiers.org/hco/1/GRCh38#225515758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181748138-A-C

225515758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181748138-A-G

225515981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181748341-T-C

225516185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181748540-G-C

225516257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181748601-T-C

225516301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181748632-C-T

225517045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181749073-T-A

225517050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181749078-T-A

225517050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181749078-T-C

225517050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181749078-T-G

http://identifiers.org/hco/1/GRCh38#225517074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181749102-C-A

225517074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181749102-C-G

225517074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181749102-C-T

225517090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181749118-T-A

225517100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181749128-T-A

225517100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181749128-T-C

http://identifiers.org/hco/1/GRCh38#225517119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181749147-C-A

225517174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181749202-G-A

225517174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181749202-G-T

225517518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 181749593-T-C

http://identifiers.org/hco/1/GRCh38#225517629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181749704-C-A

225517629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 181749704-C-T

225517749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 181749824-G-A

225517749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 181749824-G-C

225517749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 181749824-G-T

225517808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, stop_gained
orthologous variants: 181749883-G-A

225518087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181750159-T-G

225518187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181750250-T-C

225518278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181750319-A-G

225518568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181750544-T-G

225518586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181750562-G-A

225519140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, missense_variant
orthologous variants: 181751058-C-G

225519140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, missense_variant
orthologous variants: 181751058-C-T

225519151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 181751066-A-G

225519175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 181751102-A-G

225519176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, missense_variant
orthologous variants: 181751103-G-A

225519181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 181751108-G-A

225519319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181751204-T-C

225519328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181751213-C-G

225519328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181751213-C-T

225519599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181751440-T-C

225520309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181752217-A-G

225520311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181752219-T-A

225520311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181752219-T-C

225522108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181752785-T-C

225522265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181752934-C-T

225522357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181753023-G-C

225522365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181753031-C-T

225523286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181753824-C-T

http://identifiers.org/hco/1/GRCh38#225523318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181753860-A-C

http://identifiers.org/hco/1/GRCh38#225523496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181754031-A-C

225523500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181754035-C-T

225523583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181754094-G-C

225523700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181754193-T-C

225523831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181754321-C-T

225523907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181754397-T-C

225523913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181754403-G-A

225523976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181754464-C-T

225524344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181754871-T-C

225524344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181754871-T-G

225524389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181754914-C-G

225524470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181755057-G-T

225524547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181755184-G-T

225524621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 181755258-G-A

225524804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181755433-G-A

225524804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181755433-G-T

225525290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181755931-T-A

225525290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181755931-T-G

225525522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181756189-C-T

225525533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181756200-C-T

225525768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181756407-T-C

225530134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181757645-A-G

225530542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181758231-T-C

225530959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181758652-T-C

225530959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181758652-T-G

225531304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181759001-A-G

225531316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181759014-T-C

225531444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181759142-C-T

225531494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181759195-G-C

225531754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181759733-G-C

225531773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181759751-C-T

225531780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181759758-A-G

225532205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181760147-G-C

225532535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181760449-G-A

225532948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181760833-T-C

225533047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181760889-C-T

225533493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181761337-C-T

225533553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181761376-G-C

225533708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181761512-T-A

225533722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181761526-T-C

225533801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181761606-G-A

225534222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181761997-C-T

225534672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181762375-T-C

225534694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181762397-G-A

225534860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181762619-A-T

http://identifiers.org/hco/1/GRCh38#225535368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181763087-C-A

225535376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181763095-A-T

http://identifiers.org/hco/1/GRCh38#225535589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181763307-A-C

http://identifiers.org/hco/1/GRCh38#225535690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181763408-C-A

225536632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181764215-T-C

225536717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181764287-A-T

225536894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181764457-G-A

225537033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181764584-G-A

225537765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181765355-T-G

225537974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181765598-G-T

225537998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181765618-C-T

225538292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181765888-G-A

225538343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181766247-T-C

225538604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181766495-A-T

225538847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181766936-A-T

225538883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181766977-G-A

225539168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181767162-T-C

225539229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181767218-T-C

225542400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181767710-C-T

225542546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181767878-A-G

225543393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181771742-T-C

225544041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181776252-G-A

225544041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181776252-G-T

http://identifiers.org/hco/1/GRCh38#225544192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181776489-C-A

225544234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181776526-T-A

225546303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181778185-T-A

225546391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181778317-C-G

225546542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181778435-T-A

225550750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181779438-T-C

225550911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181779589-C-T

225550995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181779677-A-G

225551044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181779726-G-A

http://identifiers.org/hco/1/GRCh38#225551131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181779818-C-A

225551445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181780158-C-T

225551809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181781023-T-C

225552028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181781262-G-T

http://identifiers.org/hco/1/GRCh38#225552124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181781360-A-C

225552124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181781360-A-G

225552124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181781360-A-T

225552287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181781469-C-T

225552458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181781667-C-G

225552502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181781707-T-A

http://identifiers.org/hco/1/GRCh38#225554466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#181783322-A-C

http://identifiers.org/hco/1/GRCh38#225554479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181783336-C-A

225554479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181783336-C-T

225554481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181783338-T-C

http://identifiers.org/hco/1/GRCh38#225554763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181783859-C-A

225554763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181783859-C-T

225554864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181783937-T-C

225555109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181784163-G-A

225555109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181784163-G-T

225555806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181784485-T-C

225555906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181784623-C-T

225556320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181785034-C-T

225556808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181785424-T-C

225557101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181785687-T-G

225566027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181788028-G-A

225566505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181788417-C-T

225566564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181788475-T-C

225566708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181788618-T-C

225566881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181788792-C-G

225566961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181788878-T-C

http://identifiers.org/hco/1/GRCh38#225567599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181789620-A-C

225567637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181789646-G-C

225568666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181790865-G-C

225568666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181790865-G-T

225568908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181791065-G-A

225568908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181791065-G-C

225568935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181791093-T-C

225568935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181791093-T-G

225568936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181791094-G-A

225568941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181791099-T-C

225569111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181791261-A-G

225572763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181792602-T-C

225573256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181793077-A-G

225573501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181793274-C-T

225577507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181795316-A-G

225577587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181795382-A-G

225577656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181795449-A-G

225577744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181795525-A-G

225578062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181796065-G-A

225579714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181796877-C-T

http://identifiers.org/hco/1/GRCh38#225579730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181796894-A-C

225592011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181801640-A-G

225592157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181801781-A-G

225592338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181801955-T-G

http://identifiers.org/hco/1/GRCh38#225592407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181802011-C-A

225592436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181802036-C-G

225592507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181802144-C-T

225592619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181802396-T-A

225592621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181802398-A-G

225592715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181802492-T-C

225592983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181802754-G-A

http://identifiers.org/hco/1/GRCh38#225593105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181802819-A-C

225593105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181802819-A-G

http://identifiers.org/hco/1/GRCh38#225593149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181802879-A-C

225593222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181802963-T-C

225593400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181803094-T-G

225593401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181803095-G-C

225593401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181803095-G-T

http://identifiers.org/hco/1/GRCh38#225593427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181803112-C-A

225593427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181803112-C-G

http://identifiers.org/hco/1/GRCh38#225593452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181803139-C-A

225593922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181803557-T-C

225594124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181803943-T-C

225594267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181804176-G-T

225594330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181804477-C-G

225594646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181804768-C-G

225594646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181804768-C-T

225594727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181804846-T-A

225594928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181807730-A-G

225596097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181808608-C-T

225596265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181808769-C-G

225596379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181808857-T-A

225596471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181808929-G-A

225604351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181813943-A-G

225604522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181815535-G-A

225604542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181815554-A-G

225604555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181815567-G-A

225604555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181815567-G-C

http://identifiers.org/hco/1/GRCh38#225604559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181815571-A-C

225605130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181816234-G-A

225613323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181818373-T-C

225613681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181818675-T-C

225614422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181819092-G-C

225614443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181819113-T-A

225614457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181819128-T-C

http://identifiers.org/hco/1/GRCh38#225614478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181819149-C-A

225614489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181819162-G-C

225614589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181819262-A-G

225616775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181820294-T-G

225617231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181820418-T-C

225617319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181820511-T-C

225617419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181820628-G-A

225617484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181820737-A-G

225617814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181821047-A-G

225618227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181821439-T-A

225618250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181821462-T-C

225618688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181821725-A-T

225618791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181821819-G-A

225619199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181822141-A-G

225619748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181822784-G-A

http://identifiers.org/hco/1/GRCh38#225619888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181823198-C-A

225619929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181823256-G-C

225619975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181823307-A-T

225620006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181823339-T-C

225620124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181823453-C-G

225620213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181823540-C-T

225620637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181823654-G-A

225620637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181823654-G-C

225620684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181823703-A-G

225624727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181823813-T-C

225624864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181823938-C-T

225624993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181824038-A-G

225624995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181824040-G-A

225625104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181824151-C-T

225625115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181824162-A-T

http://identifiers.org/hco/1/GRCh38#225625123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181824216-A-C

225625199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181824419-T-A

225625363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181824581-T-C

225625416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181824797-G-A

225625416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181824797-G-T

225627351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181824987-C-G

225627548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181825167-T-A

225627548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181825167-T-C

225627633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181825249-G-A

225628773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181826103-G-A

225628894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181826205-G-A

225628894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181826205-G-T

225628924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181826226-A-G

225628943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181826245-A-G

225628959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181826261-G-A

225631120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181828339-G-C

225631291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181828514-A-G

225631635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181828555-A-G

225631754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181828710-T-C

225632135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181829460-T-C

225635588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181830860-T-C

http://identifiers.org/hco/1/GRCh38#225635590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181830862-C-A

225635752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181830984-T-C

225639013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181832885-C-T

225639035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181832907-A-G

225639039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181832911-T-C

225639091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181832959-G-C

http://identifiers.org/hco/1/GRCh38#225639177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181833050-A-C

225639346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181833200-T-A

225640048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181833835-G-A

225640306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181834093-T-C

225640345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181834132-T-C

225640589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181834351-C-T

225640690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181834442-C-T

http://identifiers.org/hco/1/GRCh38#225640817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181834599-C-A

225644269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181838720-T-C

225644372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181838795-A-T

225644780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181839364-G-A

225644780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181839364-G-C

225644811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181839387-T-C

225645154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181840065-C-G

225645156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181840067-C-G

225645156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181840067-C-T

225645583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181840662-T-C

225646182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181841246-T-G

225647399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181841821-G-A

225647667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181841981-T-C

http://identifiers.org/hco/1/GRCh38#225647806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181842119-C-A

225648005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181842233-G-A

225648014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181842242-G-T

225648595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181842848-T-G

225648671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181843044-G-C

225648671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181843044-G-T

225648822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181843157-C-T

225648914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181843271-A-G

225649259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181844071-T-C

http://identifiers.org/hco/1/GRCh38#225649372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181844187-A-C

225649872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181844824-G-A

225650306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181845126-T-G

http://identifiers.org/hco/1/GRCh38#225650871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181845416-A-C

http://identifiers.org/hco/1/GRCh38#225650873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181845418-A-C

225651482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron_variant, undefined
orthologous variants: 181845913-G-A

225652289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: intron variant
orthologous variants: 181846726-G-A

225652514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181846950-C-G

225652558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181846986-G-A

225652558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181846986-G-T

http://identifiers.org/hco/1/GRCh38#225652576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181847004-C-A

225652576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181847004-C-T

225652769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181847164-G-A

225652769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181847164-G-C

225652769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181847164-G-T

http://identifiers.org/hco/1/GRCh38#225652824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181847218-C-A

225652824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181847218-C-T

225652910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181847293-G-A

225652910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181847293-G-T

225652916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 181847298-G-A

225653024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 181847402-G-A

225653024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 181847402-G-C

http://identifiers.org/hco/1/GRCh38#225653063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181847469-C-A

225653063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 181847469-C-G

225653063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 181847469-C-T

225653065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 181847471-C-T

225653072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 181847485-G-A

http://identifiers.org/hco/1/GRCh38#225653346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18271
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181847707-C-A