49423590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125876920-A-G

49423594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125876930-T-C

49423759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125877092-G-A

49423794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125877128-T-C

49423845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125877179-T-C

49423907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125877241-T-C

http://identifiers.org/hco/15/GRCh38#49423926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125877259-C-A

49423926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125877259-C-T

49423934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125877268-T-C

49424026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 125877359-A-G

49424049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125877381-G-A

49424049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125877381-G-T

http://identifiers.org/hco/15/GRCh38#49424122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125877458-C-A

49424122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125877458-C-T

49424176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125877512-T-A

49424176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125877512-T-C

49424291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125877628-C-T

49424345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 125877682-A-G

http://identifiers.org/hco/15/GRCh38#49424601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125877945-C-A

http://identifiers.org/hco/15/GRCh38#49424618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125877960-C-A

49424651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125877992-G-A

49424651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125877992-G-T

49424730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125878071-A-G

http://identifiers.org/hco/15/GRCh38#49424750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125878090-C-A

49424750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125878090-C-G

49424817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125878145-T-C

49424872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125878203-T-A

http://identifiers.org/hco/15/GRCh38#49424877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125878208-C-A

49424877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125878208-C-T

49424917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125878245-G-A

49425231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125878546-T-C

49425330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125878643-C-T

49425486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125878798-A-G

49425568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125878874-A-G

http://identifiers.org/hco/15/GRCh38#49425630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125878922-C-A

49425724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125879011-G-A

49425757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125879043-G-A

49425986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125879178-A-T

49426142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125879243-A-G

49426224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125879304-A-G

49426440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125879537-C-T

49426475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125879578-T-C

49426697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125879793-T-C

http://identifiers.org/hco/15/GRCh38#49426745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125879831-A-C

49426745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron variant
orthologous variants: 125879831-A-G

49426856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125879950-T-C

49427171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125880226-C-G

49427346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125880406-A-T

49427603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125880624-G-A

49427767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125880828-C-T

49427821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125880880-C-G

49427821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125880880-C-T

49428670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125881530-C-T

49428803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125881678-G-A

49429226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125882109-T-C

49429851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125882991-G-A

49429851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125882991-G-C

49429900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125883042-A-G

49429919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125883061-A-G

49429962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125883119-C-T

http://identifiers.org/hco/15/GRCh38#49430962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125883637-C-A

49431002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125883667-A-T

49432127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125884198-C-T

49432202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125884270-G-T

49432430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125884493-G-A

49433111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125885177-G-C

49433173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125885211-T-C

49433930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125885857-C-T

49434346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125886621-C-T

49435160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125887443-T-C

49435213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125887481-C-T

49435243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125887509-G-A

49435510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125887654-T-A

49435558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125887699-T-C

http://identifiers.org/hco/15/GRCh38#49436055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125888335-C-A

49436336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125888581-T-C

49436336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125888581-T-G

49436378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125888646-T-C

49436593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125888938-T-C

49436593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125888938-T-G

49436600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125888945-T-C

49436698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125889058-G-T

49436946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125889302-C-G

http://identifiers.org/hco/15/GRCh38#49437039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125889401-C-A

49437132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125889484-T-C

49437802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125889847-A-G

49441915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125892254-A-G

49441984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125892328-G-A

49442094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125892424-T-C

49442461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125892771-T-C

49442552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125892849-T-G

49442584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125892876-C-T

49442598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125892890-A-G

http://identifiers.org/hco/15/GRCh38#49442656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125892948-C-A

49442784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125893262-A-G

49445516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125894265-T-C

49445948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125894514-T-A

49445961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125894527-T-C

49446518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125894867-G-A

49447078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125895341-G-A

49447208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125895444-T-C

49450818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125898383-A-G

49451087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125898606-C-G

49455292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125902042-A-G

49455466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125902264-C-T

49455670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125902429-T-C

49455690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125902449-A-T

49455941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125902710-G-C

49456196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125902973-T-C

49456196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125902973-T-G

49456234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125903011-T-C

49456306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125903083-T-C

49456478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125903257-T-C

http://identifiers.org/hco/15/GRCh38#49456658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125903441-A-C

49456658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125903441-A-G

49457132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125903828-G-C

49457387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125904167-T-A

49457387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125904167-T-C

49457531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125904315-G-C

49457580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125904368-T-C

49457991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125904764-A-G

http://identifiers.org/hco/15/GRCh38#49458050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125904812-A-C

49458065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125904827-T-C

49458330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125904976-A-G

49458492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125905135-A-G

49458648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125905289-T-C

49458690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125905331-C-T

49458720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125905361-T-A

49459297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125906239-T-C

49459297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125906239-T-G

49459378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125906316-T-C

49459389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125906324-C-T

49459511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125906428-A-G

49459843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125906738-A-G

49459843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125906738-A-T

49459913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125906818-G-A

49460553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125907454-C-G

49460553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125907454-C-T

49460628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125907529-C-G

49461236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125908073-G-C

49462613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125910548-T-C

49463099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125911117-A-G

49463149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125911158-T-C

http://identifiers.org/hco/15/GRCh38#49463512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125911287-C-A

49463512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125911287-C-T

http://identifiers.org/hco/15/GRCh38#49464062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125911703-C-A

49464062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125911703-C-T

49464090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125911720-T-C

49464193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125911813-C-T

49464643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125912609-C-T

49464843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125912803-A-G

49464891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125912874-C-T

49464949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125912937-G-A

49465716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125913307-C-T

49466803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125914114-T-A

49466803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125914114-T-C

49467393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125914476-G-C

49467393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125914476-G-T

49467761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125914804-A-G

49467970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125914924-G-T

49469171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125915843-C-T

49469729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125916355-T-C

49469808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125916415-G-T

49469893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125916466-T-C

49469949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125916523-A-T

http://identifiers.org/hco/15/GRCh38#49470104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125916613-C-A

49470480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125916908-C-T

49470812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125917753-G-C

49470841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125917782-A-T

49474433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125922179-G-T

http://identifiers.org/hco/15/GRCh38#49475988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125925175-C-A

49476056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125925217-C-T

http://identifiers.org/hco/15/GRCh38#49476247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125925387-C-A

49476247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125925387-C-G

49476247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125925387-C-T

49476280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125925420-T-C

http://identifiers.org/hco/15/GRCh38#49476347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125925493-A-C

49476488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125925633-A-T

http://identifiers.org/hco/15/GRCh38#49476627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125925759-A-C

49478446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125926732-G-A

49478992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125927300-G-A

49479038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125927325-C-T

49479214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125927447-G-A

49481467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125928348-G-A

http://identifiers.org/hco/15/GRCh38#49481543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125928429-C-A

49481697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125928562-C-T

49482487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125929622-G-A

49482823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125929939-G-A

49482951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125930046-G-A

49482980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125930074-C-G

49483132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125930136-T-C

http://identifiers.org/hco/15/GRCh38#49483351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125930341-C-A

49483534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125930525-A-G

49483628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125930618-A-G

49483700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125930690-C-G

49483797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125930786-A-G

49484394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125931371-A-G

http://identifiers.org/hco/15/GRCh38#49484776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125931760-A-C

http://identifiers.org/hco/15/GRCh38#49484779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125931762-A-C

49484779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125931762-A-T

49485036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125932006-C-G

49485067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125932036-A-G

49485078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125932045-A-G

49485125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125932096-T-A

49485585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125932541-A-G

49485637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125932592-A-T

49485711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125932666-A-G

49485714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125932669-C-T

49485715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125932670-T-C

49486240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125933116-A-G

49486568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125933452-A-G

49486696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125933566-G-T

49487545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125934482-G-C

49487787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125935457-A-G

49487933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125935589-G-T

49488736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3685
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125936461-T-C