26867018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57159845-G-T

26867048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57159812-A-G

26867173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57159687-C-T

26867176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57159684-G-A

26867217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57159643-G-A

26867217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57159643-G-T

26867284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57159576-G-A

26867284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57159576-G-T

http://identifiers.org/hco/15/GRCh38#26867373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57159497-C-A

26867499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57159441-G-A

26867499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57159441-G-T

26867525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57159426-A-G

26867541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57159411-G-A

26867596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57159360-G-C

26867596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57159360-G-T

http://identifiers.org/hco/15/GRCh38#26867657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57159307-C-A

26867664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57159297-G-C

26867884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57159112-G-A

26867936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57159064-G-A

26867955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57159052-A-G

http://identifiers.org/hco/15/GRCh38#26867971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57159038-C-A

26867971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57159038-C-T

http://identifiers.org/hco/15/GRCh38#26868042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57158981-C-A

26868042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57158981-C-T

http://identifiers.org/hco/15/GRCh38#26868073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57158950-C-A

26868073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57158950-C-T

http://identifiers.org/hco/15/GRCh38#26868119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57158905-C-A

26868119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57158905-C-T

26868205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57158815-T-A

26868270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57158751-C-G

26868389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57158639-G-A

26868389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57158639-G-C

26868389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57158639-G-T

26868642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57158383-A-G

http://identifiers.org/hco/15/GRCh38#26868934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57158116-C-A

26868934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57158116-C-T

26869017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57158037-T-G

26869103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57157951-T-C

26869103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57157951-T-G

http://identifiers.org/hco/15/GRCh38#26869126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57157932-C-A

26869126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57157932-C-G

26869224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57157835-G-A

26869224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57157835-G-C

http://identifiers.org/hco/15/GRCh38#26869352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57157707-C-A

26871479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57155781-T-C

26871512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57155744-G-A

http://identifiers.org/hco/15/GRCh38#26871536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57155713-A-C

26871615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57155647-A-G

26871656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57155607-G-A

26871731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57155532-A-G

26872586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57154181-T-C

26872878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57153887-T-C

26872882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57153883-T-C

26872939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57153824-T-C

http://identifiers.org/hco/15/GRCh38#26873042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57153728-A-C

http://identifiers.org/hco/15/GRCh38#26873047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57153723-A-C

26873574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57153238-T-A

26873601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57153205-C-T

http://identifiers.org/hco/15/GRCh38#26873608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57153198-A-C

26873616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57153190-C-G

26873652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57153159-T-C

26873758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57153055-C-T

26873844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57152950-A-G

26873990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57152819-T-A

26874034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57152765-C-T

26874070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57152732-G-A

26874094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57152703-A-G

26874121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57152619-G-A

26874121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57152619-G-C

26874121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57152619-G-T

26874348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57152429-A-G

26874381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57152394-A-G

26874660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57152128-C-G

26874660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57152128-C-T

http://identifiers.org/hco/15/GRCh38#26874748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57152077-A-C

26874761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57152069-T-C

26874951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57151915-G-A

26875050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57151842-G-A

26875204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57151754-C-T

26875210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57151752-G-C

26875244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57151723-G-A

26875322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57151645-A-G

26875614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57151361-C-T

26875642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57151293-G-A

26875643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57151292-C-T

26876059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57150641-G-T

26876070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57150630-G-T

26876235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57150509-G-A

26876248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57150496-T-C

26876299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57150465-A-T

26876353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57150422-C-T

26876964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57149720-C-T

26877213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57149496-G-C

http://identifiers.org/hco/15/GRCh38#26877365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57149387-C-A

http://identifiers.org/hco/15/GRCh38#26877585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57149179-C-A

http://identifiers.org/hco/15/GRCh38#26877680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57149075-C-A

26877680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57149075-C-T

26877681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57149074-A-G

26877782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57144851-A-G

26877961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57144681-C-T

26877975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57144663-G-A

26877975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57144663-G-T

26878012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57144636-T-G

26878210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57144496-G-A

26878272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57144449-T-C

http://identifiers.org/hco/15/GRCh38#26878273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57144448-A-C

26878299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57144423-T-C

26878680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57144087-A-G

26878715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57144051-T-C

26878830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57143707-A-G

26878922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57143610-G-A

26878923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57143609-T-A

http://identifiers.org/hco/15/GRCh38#26878967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57143577-C-A

26879064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57143460-T-C

26879083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57143442-G-A

26879137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57142659-A-G

26879229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57142571-T-C

26879323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57142476-T-A

26880098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57141488-C-T

26880153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57141302-T-G

26880305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57141130-G-A

26880313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57141123-C-G

26880602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57140859-G-A

26880602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57140859-G-T

26880726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57140728-G-A

26880726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57140728-G-T

26880996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57140460-G-C

http://identifiers.org/hco/15/GRCh38#26881006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57140450-A-C

26881006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57140450-A-G

http://identifiers.org/hco/15/GRCh38#26881030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57140432-A-C

26881303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57140225-G-A

26882079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57139880-C-T

26882430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57139545-T-C

26882701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57139313-G-A

26883013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57139088-T-A

http://identifiers.org/hco/15/GRCh38#26883058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57139048-A-C

26883063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57139040-C-G

26883078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57139025-G-A

26883078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57139025-G-T

26883104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57138999-G-A

26883104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57138999-G-T

26883219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57138887-T-A

26883244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57138862-G-A

26883293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57138800-A-G

26883310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57138795-A-T

26883409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57138696-C-T

http://identifiers.org/hco/15/GRCh38#26883469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57138636-A-C

26883469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57138636-A-G

26883532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57138573-G-A

26883532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57138573-G-T

26883538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57138567-A-G

http://identifiers.org/hco/15/GRCh38#26883580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57138518-C-A

26883580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57138518-C-G

26883580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57138518-C-T

http://identifiers.org/hco/15/GRCh38#26883641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57138460-C-A

26883641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57138460-C-T

26883666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57138421-A-G

26883692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57138400-T-C

26883693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57138399-T-C

26883707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57138385-T-C

26884280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57138137-C-T

26884390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57138043-T-C

26884406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57138027-G-C

26886397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57137223-G-A

http://identifiers.org/hco/15/GRCh38#26886407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57137213-C-A

26888406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57133821-G-A

26888435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57133796-G-A

26888548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57133691-T-C

26888756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57133534-C-T

26888846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57133445-T-C

26889071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57133243-G-C

26906625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57112209-A-T

http://identifiers.org/hco/15/GRCh38#26906933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57111919-A-C

http://identifiers.org/hco/15/GRCh38#26907245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57111471-A-C

26907350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57111377-A-G

26907434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57111305-G-A

26907793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57110980-C-T

http://identifiers.org/hco/15/GRCh38#26909752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57107595-C-A

26909855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57107497-A-G

26909983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57107412-A-G

26910624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57107081-T-G

26910692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57107021-T-C

26910807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57106904-T-C

26910828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57106885-G-A

http://identifiers.org/hco/15/GRCh38#26910887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57106823-C-A

26911294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57106463-A-G

26911294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57106463-A-T

26911323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57106445-C-T

http://identifiers.org/hco/15/GRCh38#26911504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57106309-C-A

26911551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57106268-G-A

26911568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57106252-T-C

26911577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57106244-A-G

26911632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57106188-C-G

26911784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57106046-G-A

26911831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57106000-C-T

26912504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57105027-T-C

26912561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57104971-T-A

26912760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57104791-A-T

26912841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57104701-T-C

26913286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57104448-G-A

26913345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57104395-G-C

http://identifiers.org/hco/15/GRCh38#26913346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57104394-A-C

26913458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57104300-T-A

26913458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57104300-T-G

26913641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57104132-G-A

26914136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57103286-T-A

26914136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57103286-T-C

26914418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57103132-T-C

26914499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57103048-G-A

26914561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57102982-T-C

26914697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57102854-A-G

http://identifiers.org/hco/15/GRCh38#26914745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57102804-C-A

26914745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57102804-C-T

26914861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant
orthologous variants: 57102715-G-A

26914916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57102659-A-T

26914942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57102636-A-G

26914942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57102636-A-T

26914978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57102600-A-T

26914984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57102598-A-G

26914985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57102597-T-C

http://identifiers.org/hco/15/GRCh38#26914992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57102590-C-A

26914992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57102590-C-T

26915011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57102572-G-A

26915011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57102572-G-T

http://identifiers.org/hco/15/GRCh38#26915028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57102554-C-A

26915100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57102489-A-G

26915132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57102459-G-A

26915151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57102437-G-A

http://identifiers.org/hco/15/GRCh38#26915171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57102417-A-C

http://identifiers.org/hco/15/GRCh38#26915173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57102415-C-A

26915173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57102415-C-T

26915397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57102138-C-G

26915436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57102063-A-T

26925987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57099645-T-C

26926034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57099598-C-G

26926034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57099598-C-T

26926050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57099580-T-A

26926051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57099579-G-A

26926051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57099579-G-T

26926075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57099556-T-A

26926210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57099460-T-C

26926398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57099312-G-T

26926661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57099054-T-C

26926730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57098989-A-G

26927012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57098700-A-G

26927131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57098618-T-C

26927226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57098591-C-T

26927498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57098501-A-G

26927602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57098417-G-C

http://identifiers.org/hco/15/GRCh38#26927678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57098343-A-C

26927693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57098323-A-T

26927734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57098280-C-G

26927853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57098169-A-G

26927993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57098049-T-C

26928169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57097873-G-T

26928394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57097692-G-A

26928518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57097573-T-G

26928648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57097434-G-A

26928670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57097412-A-G

26928793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57097255-A-G

26928794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57097254-G-A

26928871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57097175-G-A

26928888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57097160-G-A

26928890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57097158-G-C

26928890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57097158-G-T

26928943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57097107-G-A

26936799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57071979-G-A

26936799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57071979-G-T

26937092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57071719-T-C

http://identifiers.org/hco/15/GRCh38#26937098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57071713-C-A

26937098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57071713-C-T

http://identifiers.org/hco/15/GRCh38#26937322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57071495-A-C

26937322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant
orthologous variants: 57071495-A-G

26937349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57071473-G-A

26937349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57071473-G-C

26937369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57071454-G-A

26937646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57071182-C-T

26937723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57071107-T-G

26937845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57071007-A-G

26937921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57070938-G-A

26938378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57070527-G-A

26938433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57070494-T-C

26938567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57070363-C-T

26938947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57070009-T-A

26938985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57069968-T-A

26938985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57069968-T-G

26939028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57069919-C-G

26939079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57069865-A-G

26939121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57069819-C-G

26939135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57069805-A-G

http://identifiers.org/hco/15/GRCh38#26939324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57069633-C-A

26939324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant
orthologous variants: 57069633-C-T

26939382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant
orthologous variants: 57069575-G-A

26939382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant
orthologous variants: 57069575-G-C

26939428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant
orthologous variants: 57069532-C-G

26939444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57069516-T-A

26939551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57069426-A-G

26939551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57069426-A-T

26939617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57069355-G-C

http://identifiers.org/hco/15/GRCh38#26939619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57069353-C-A

26939619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57069353-C-G

26939619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57069353-C-T

26939846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57068197-G-A

26939846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57068197-G-T

26939878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57068172-A-T

http://identifiers.org/hco/15/GRCh38#26939880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57068170-C-A

http://identifiers.org/hco/15/GRCh38#26939881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57068169-A-C

26939881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57068169-A-G

26940096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57067947-G-A

26940096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57067947-G-T

http://identifiers.org/hco/15/GRCh38#26940106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57067937-C-A

26940106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57067937-C-T

26940109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57067934-G-C

26940641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57066806-A-T

26940906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57065431-T-C

26941193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57065189-G-T

26941338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57065053-G-A

26941406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57064993-T-A

26942020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57064395-A-T

26942115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57064308-G-A

26942115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57064308-G-T

26942208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57064223-C-T

26942230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57064201-C-T

26942250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57064181-G-A

26942362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57064107-C-T

26942565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57063908-A-G

26942606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57063864-C-T

26942675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57063798-G-C

26943132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57063618-T-A

26943132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57063618-T-C

26943137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57063613-G-A

26943137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57063613-G-T

26943156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57063601-T-C

26943203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57063555-T-A

26943203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron variant
orthologous variants: 57063555-T-C

26943346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, stop_gained
orthologous variants: 57063412-G-T

26943352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant
orthologous variants: 57063406-G-T

26943358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant
orthologous variants: 57063400-G-A

26943358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, missense_variant
orthologous variants: 57063400-G-T

26943455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: intron_variant, splice_acceptor_variant
orthologous variants: 57063300-A-G

26943506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57063246-G-A

26943506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57063246-G-T

26943521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57063231-T-A

26943521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57063231-T-C

26943784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062970-G-A

26943784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062970-G-T

26943921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062800-C-T

26944015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062674-G-A

26946132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57060093-C-T

26946143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57060082-G-C

26946242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57059983-A-G

26946397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57059818-T-C

26946402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57059813-G-C

26946402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57059813-G-T

26946523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57059693-G-C

26946620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57059597-A-G

26946668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57059563-C-T

26946684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57059547-C-T

26946813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57059409-G-A

26947021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57059217-T-C

26947092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57059143-T-C

26947177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57058866-C-T

26947178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57058865-G-A

26947827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57058751-G-A

26947827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57058751-G-T

http://identifiers.org/hco/15/GRCh38#26947831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57058747-A-C

26947908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57058678-C-G

26948216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 57058370-G-A

26948216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 57058370-G-C

26948242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: 57058352-A-G

26948289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: 57058316-G-A

26948289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: 57058316-G-T

http://identifiers.org/hco/15/GRCh38#26948296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57058309-C-A

http://identifiers.org/hco/15/GRCh38#26948310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57058293-C-A

26948310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: 57058293-C-T

http://identifiers.org/hco/15/GRCh38#26948496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57058110-C-A

26948496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: 57058110-C-T

26948575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: 57058038-G-A

26948575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: 57058038-G-C

http://identifiers.org/hco/15/GRCh38#26948913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57057690-C-A

26948959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: 57057641-G-A

26948969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: 57057631-A-G

26949025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: 57057573-T-C

26949047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: 57057556-T-C

26949072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: 57057541-G-T

http://identifiers.org/hco/15/GRCh38#26949201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#57057411-C-A

26949201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4079
most severe consequence: 3 prime UTR variant
orthologous variants: 57057411-C-T