37201761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79227307-A-G

37201945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79227476-A-G

37201973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79227493-T-A

37201973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79227493-T-C

http://identifiers.org/hco/2/GRCh38#37201984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79227504-A-C

37201984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79227504-A-G

http://identifiers.org/hco/2/GRCh38#37202006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79227516-C-A

37202077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79227557-G-A

37202077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79227557-G-T

37202162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79227628-G-A

37202162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79227628-G-C

37202162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79227628-G-T

37202521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79227862-T-A

37202521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79227862-T-C

37202630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79227915-G-A

37202630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79227915-G-T

http://identifiers.org/hco/2/GRCh38#37202879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79228080-A-C

37202920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79228121-T-C

http://identifiers.org/hco/2/GRCh38#37202923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79228124-C-A

http://identifiers.org/hco/2/GRCh38#37202930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79228131-A-C

37202930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79228131-A-G

37203016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79228217-A-T

37203033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79228233-T-A

37203033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79228233-T-C

37203300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79228308-A-G

37203442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79228448-C-T

37210926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79228983-T-C

http://identifiers.org/hco/2/GRCh38#37210932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79228986-C-A

37210932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79228986-C-G

37210932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79228986-C-T

37210941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79228995-A-G

37210941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79228995-A-T

37210952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229014-T-A

37210952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229014-T-C

37210988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229053-T-C

37211031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229096-G-A

37211069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79229134-G-A

37211075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229140-T-A

37211075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79229140-T-C

http://identifiers.org/hco/2/GRCh38#37211124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79229193-A-C

37211124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229193-A-G

http://identifiers.org/hco/2/GRCh38#37211678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79229461-C-A

37211803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229521-A-G

37211808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229526-G-A

37211808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229526-G-T

37211848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229564-A-G

37211858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229574-T-C

37211946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79229659-A-G

37212006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79229713-A-G

37212006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229713-A-T

37212023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229730-T-A

37212234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229841-A-G

37212234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229841-A-T

37212279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229888-G-A

37212279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229888-G-T

37212287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229899-T-C

37212288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229900-T-C

http://identifiers.org/hco/2/GRCh38#37212302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79229913-A-C

37212323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229931-G-A

37212323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229931-G-C

37212324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79229932-A-G

37212328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79229936-A-G

37212398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79230006-A-G

37212485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79230094-T-C

37212578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79230156-T-C

http://identifiers.org/hco/2/GRCh38#37213794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79230596-C-A

37213886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 79230687-A-T

37213928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79230729-T-C

37213974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79230781-T-C

http://identifiers.org/hco/2/GRCh38#37214093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79230862-C-A

37214387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79231449-A-G

37214825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79231823-T-G

37214877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79231866-G-A

37214877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79231866-G-T

37215000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79231973-T-C

37215004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79231977-T-G

http://identifiers.org/hco/2/GRCh38#37215013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79231985-C-A

37215013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79231985-C-G

37215073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79232106-G-A

37215073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79232106-G-C

37215073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79232106-G-T

37215074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79232107-T-C

37215074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79232107-T-G

37215240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79232257-T-C

37215244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79232261-G-A

37215244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79232261-G-T

37215361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79232626-G-A

37215362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79232627-G-A

37215362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79232627-G-T

37215498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79232791-A-T

37215518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 79232808-G-A

37215518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 79232808-G-C

http://identifiers.org/hco/2/GRCh38#37215841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79233177-C-A

37215841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79233177-C-T

37216113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 79233316-T-C

37216152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79233355-G-A

37216201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: synonymous variant
orthologous variants: 79233404-T-A

http://identifiers.org/hco/2/GRCh38#37216286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79233480-A-C

37216463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79233665-C-G

37216463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79233665-C-T

37216489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79233690-G-A

37216489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79233690-G-T

37217076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79234389-G-A

37217076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79234389-G-T

37217525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79234718-T-A

37220372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79236694-G-A

37220372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79236694-G-T

37220404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79236726-C-G

37220526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79236838-G-A

37220526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79236838-G-C

37220526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79236838-G-T

37220685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79237003-C-G

37220685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79237003-C-T

37221720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79237761-C-G

37221805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79237836-A-G

37221806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79237837-C-T

37221808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79237839-T-C

37221859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79237890-T-C

37222007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79238029-G-C

37222412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79238771-A-G

37222435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79238794-A-T

37222459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: synonymous variant
orthologous variants: 79238818-T-C

37222487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79238852-T-C

http://identifiers.org/hco/2/GRCh38#37222521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/17/GRCm39#79238886-C-A

37222521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79238886-C-T

37222531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: synonymous variant
orthologous variants: 79238896-T-A

http://identifiers.org/hco/2/GRCh38#37222561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79238923-C-A

37222561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 79238923-C-G

37222561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 79238923-C-T

37222570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79238932-A-G

37222574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79238935-T-C

37222578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79238939-G-C

37222610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79238995-T-C

37222615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239000-T-A

37222629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239014-C-T

37222644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239029-A-G

37222655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239044-T-C

37222671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239060-A-G

37222681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239070-T-G

37222855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239210-T-C

37222855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239210-T-G

37222899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239262-C-G

37222900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239263-T-C

37222935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239297-C-G

37222987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239358-T-A

37223088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239451-G-T

37223102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239464-A-T

37223124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239489-T-A

37223124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239489-T-C

37223236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: synonymous variant
orthologous variants: 79239605-A-G

37223338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: stop gained
orthologous variants: 79239707-G-T

37223359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: synonymous variant
orthologous variants: 79239728-A-G

37223359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: synonymous variant
orthologous variants: 79239728-A-T

37223426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239795-T-C

37223443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79239812-A-T

http://identifiers.org/hco/2/GRCh38#37223538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79239918-C-A

37223636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79240008-G-C

37223708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79240153-A-G

37223946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79240437-T-C

37226716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79241149-C-T

http://identifiers.org/hco/2/GRCh38#37226802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79241262-C-A

37226802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79241262-C-G

37226802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79241262-C-T

37226902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79241469-A-G

37226950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79241520-C-T

http://identifiers.org/hco/2/GRCh38#37226963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79241533-A-C

37227276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79241808-G-A

37227276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79241808-G-C

37227479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79241954-A-T

37227495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79241970-T-C

37227495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79241970-T-G

37227512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79241983-T-C

37227532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79241992-G-T

http://identifiers.org/hco/2/GRCh38#37227693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79242153-A-C

http://identifiers.org/hco/2/GRCh38#37227928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79242388-C-A

37227928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79242388-C-T

http://identifiers.org/hco/2/GRCh38#37228062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79242522-A-C

37228241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: synonymous variant
orthologous variants: 79242701-A-G

http://identifiers.org/hco/2/GRCh38#37228295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79242755-C-A

37228295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79242755-C-G

37228295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79242755-C-T

37228605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: synonymous variant
orthologous variants: 79243065-G-C

37228606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79243066-G-A

37228606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79243066-G-C

37228606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79243066-G-T

37228670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: synonymous variant
orthologous variants: 79243130-A-G

http://identifiers.org/hco/2/GRCh38#37228701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79243164-C-A

37228727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79243190-T-C

37228727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79243190-T-G

37228733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79243196-T-A

37228733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79243196-T-C

37228751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79243208-G-A

37228760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79243217-G-A

37228785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: synonymous variant
orthologous variants: 79243242-A-T

http://identifiers.org/hco/2/GRCh38#37228856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79243319-A-C

37228856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79243319-A-G

37228856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense variant
orthologous variants: 79243319-A-T

http://identifiers.org/hco/2/GRCh38#37229049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79243506-C-A

37229049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79243506-C-G

37229076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79243532-G-A

37229076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79243532-G-T

37229092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79243548-A-T

37229118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron variant
orthologous variants: 79243570-T-A

37231257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, undefined
orthologous variants: 79244206-G-A

37231257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, undefined
orthologous variants: 79244206-G-C

37231257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, undefined
orthologous variants: 79244206-G-T

37231262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, undefined
orthologous variants: 79244211-G-A

37231262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, undefined
orthologous variants: 79244211-G-T

http://identifiers.org/hco/2/GRCh38#37231268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79244217-C-A

37231268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: intron_variant, undefined
orthologous variants: 79244217-C-T

37231303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79244248-G-C

http://identifiers.org/hco/2/GRCh38#37231311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79244256-C-A

37231311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79244256-C-G

37231311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79244256-C-T

37231461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense_variant, undefined
orthologous variants: 79244353-G-A

37231461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense_variant, undefined
orthologous variants: 79244353-G-C

37231471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense_variant, undefined
orthologous variants: 79244363-T-A

37231471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense_variant, undefined
orthologous variants: 79244363-T-C

37231471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense_variant, undefined
orthologous variants: 79244363-T-G

37231519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: missense_variant, undefined
orthologous variants: 79244411-G-A

37231572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79244464-G-A

37231572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79244464-G-C

37231589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24218
most severe consequence: 5 prime UTR variant
orthologous variants: 79244479-T-A