31498177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 5 prime UTR variant
orthologous variants: 20691286-G-T

http://identifiers.org/hco/18/GRCh38#31498205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#20691313-C-A

31498205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 20691313-C-T

http://identifiers.org/hco/18/GRCh38#31498379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20691422-C-A

31498379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20691422-C-G

31498379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20691422-C-T

31498407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20691450-G-A

31498407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20691450-G-C

31498407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20691450-G-T

http://identifiers.org/hco/18/GRCh38#31498553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#20691545-A-C

31498553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, undefined
orthologous variants: 20691545-A-T

31498626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, undefined
orthologous variants: 20691606-G-T

31498683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, undefined
orthologous variants: 20691658-C-T

31498883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20691832-T-C

http://identifiers.org/hco/18/GRCh38#31499025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20691975-C-A

31499064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20692022-T-C

31499500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20692544-C-T

31499828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20692834-T-G

31499831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20692840-A-G

31500696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20694121-A-G

31500791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20694203-G-T

31500809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20694220-G-C

31501010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20694432-C-T

http://identifiers.org/hco/18/GRCh38#31501017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20694439-A-C

31501813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20695131-C-T

http://identifiers.org/hco/18/GRCh38#31501840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20695148-C-A

31502149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20695423-T-G

31504577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20698118-A-G

31504676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20698227-G-C

31504925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20698409-A-G

31505064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20698518-G-A

31505110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20698552-A-G

31505125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20698565-A-G

31506362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20699882-C-T

31506371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20699891-A-G

31506657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20700130-T-C

31506689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20700173-T-G

31506706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20700190-G-T

31506712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20700196-T-G

http://identifiers.org/hco/18/GRCh38#31506783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20700270-C-A

31506800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20700289-A-G

http://identifiers.org/hco/18/GRCh38#31508820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20700763-A-C

31508955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20700895-G-A

31509638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20702064-T-G

http://identifiers.org/hco/18/GRCh38#31509649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20702080-A-C

31509721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20702155-G-A

31509742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20702174-G-A

31509891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20702316-T-G

31510250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20703344-T-A

http://identifiers.org/hco/18/GRCh38#31510513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#20703600-C-A

31510562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, undefined
orthologous variants: 20703659-T-C

http://identifiers.org/hco/18/GRCh38#31510711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20703778-C-A

31514923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20704099-T-A

31517918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20705749-C-T

http://identifiers.org/hco/18/GRCh38#31518305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20706605-C-A

31518305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20706605-C-T

31518316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20706615-G-A

31518374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20706673-T-C

31518471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20706765-G-A

31518668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20706953-G-C

31518718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20707011-G-A

31518767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20707073-T-A

31518844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20707146-C-T

31519084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20707394-G-A

31519108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20707417-C-T

http://identifiers.org/hco/18/GRCh38#31519710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20707915-C-A

31519710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20707915-C-T

31519901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20708095-G-A

31519904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20708098-A-T

http://identifiers.org/hco/18/GRCh38#31520006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20708206-C-A

31520006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20708206-C-G

http://identifiers.org/hco/18/GRCh38#31520043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20708244-C-A

31520058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20708259-T-C

31520066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20708267-A-G

31520066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20708267-A-T

http://identifiers.org/hco/18/GRCh38#31520159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20708329-A-C

31520159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20708329-A-T

31520210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20708376-C-T

31520331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20708520-A-T

31520507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20708711-G-A

31520830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20712124-G-A

31520986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20712281-T-A

31520986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20712281-T-G

31521006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20712297-T-C

31521129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20712421-A-G

31521268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20712696-A-T

31521338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20712793-T-G

31521342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20712797-G-A

http://identifiers.org/hco/18/GRCh38#31521389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20712849-C-A

31521389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20712849-C-G

31521389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20712849-C-T

31521433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20712891-A-G

31521454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20712910-T-C

31521613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20713065-T-A

http://identifiers.org/hco/18/GRCh38#31521742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20713188-C-A

31521840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20713266-G-C

31521849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20713275-C-T

31521882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20713304-C-T

http://identifiers.org/hco/18/GRCh38#31522038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20713525-C-A

31522058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20713544-T-C

31522105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20713591-T-G

31522370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20713854-G-T

31522388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 20713869-G-T

http://identifiers.org/hco/18/GRCh38#31522578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20714063-C-A

31523759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20714994-C-T

31524087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20715393-A-G

http://identifiers.org/hco/18/GRCh38#31524312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20715611-C-A

31524331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20715630-T-C

31524368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20715675-G-A

31524376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20715683-G-A

31524378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20715685-A-T

31524384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20715691-A-G

31524385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20715692-C-T

31524432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20715741-T-C

31524636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20715943-T-G

31524649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20715956-A-G

31524662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20715957-G-A

31524662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20715957-G-T

31524686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20715977-G-A

31524699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 20715990-G-A

31524699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 20715990-G-T

http://identifiers.org/hco/18/GRCh38#31524700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20715991-C-A

31524762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20716053-C-G

31524762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20716053-C-T

31524915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20716206-G-A

31524915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20716206-G-C

31524934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20716223-G-A

31524934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20716223-G-C

http://identifiers.org/hco/18/GRCh38#31524965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20716252-C-A

31524967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20716254-C-G

31524974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20716261-G-A

31524985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20716272-A-G

http://identifiers.org/hco/18/GRCh38#31524988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20716275-C-A

31524988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20716275-C-T

31524989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20716279-A-G

31524989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20716279-A-T

31525069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20716358-T-C

http://identifiers.org/hco/18/GRCh38#31525775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20716532-A-C

http://identifiers.org/hco/18/GRCh38#31525788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20716548-A-C

31525794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20716552-G-T

31530917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20722935-T-C

31530918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20722936-G-T

31530924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20722942-G-A

31530924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20722942-G-T

31531076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20723094-C-T

31531279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20723297-T-C

31533846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20724299-C-T

31533978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20724549-A-T

31535171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20724797-A-G

31536087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20725214-A-G

31536150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20725277-G-A

31536150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20725277-G-C

31536160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20725287-A-G

31536252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: missense variant
orthologous variants: 20725379-A-G

31536272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: synonymous variant
orthologous variants: 20725399-A-G

31536351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: missense variant
orthologous variants: 20725478-A-G

31536358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: missense variant
orthologous variants: 20725485-G-A

31536417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: missense variant
orthologous variants: 20725544-G-A

31536418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: missense variant
orthologous variants: 20725545-C-T

31536457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20725576-A-G

31536498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20725623-G-A

http://identifiers.org/hco/18/GRCh38#31536567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20725697-C-A

31538598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20726989-T-C

31538642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20727043-T-A

31538642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20727043-T-C

31538708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20727079-G-A

http://identifiers.org/hco/18/GRCh38#31538742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20727113-A-C

31538746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 20727116-T-A

31538746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 20727116-T-C

31538781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: missense variant
orthologous variants: 20727151-A-G

31538785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: synonymous variant
orthologous variants: 20727155-G-A

31538806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: synonymous variant
orthologous variants: 20727176-G-A

31538806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: missense variant
orthologous variants: 20727176-G-C

31538806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: missense variant
orthologous variants: 20727176-G-T

31539300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20727374-A-G

http://identifiers.org/hco/18/GRCh38#31539329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20727395-A-C

31539364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20727430-T-A

31539364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20727430-T-G

31539436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20727493-G-A

31539592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20727629-A-G

31539592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20727629-A-T

31539677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20727689-G-A

31540405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20727835-C-T

31540470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20727901-G-A

31540474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20727905-C-G

31540483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20727914-G-A

31540884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20728717-A-T

31541005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20728821-C-T

31541008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20728824-G-A

31541008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20728824-G-C

31541054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20728870-G-T

31541065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20728903-G-C

31541112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20728952-G-A

31541112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20728952-G-T

http://identifiers.org/hco/18/GRCh38#31541200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20729024-A-C

31541200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: synonymous variant
orthologous variants: 20729024-A-G

31541233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: synonymous variant
orthologous variants: 20729057-C-T

31541434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20729655-T-G

31541461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20729682-G-A

31541461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20729682-G-T

31542001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20730891-G-A

31542001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20730891-G-T

31542038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20730924-T-A

31542038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: 20730924-T-G

http://identifiers.org/hco/18/GRCh38#31542145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20731023-C-A

http://identifiers.org/hco/18/GRCh38#31542274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20731140-A-C

31542274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20731140-A-G

31542577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20731453-G-T

31542860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 20731733-T-C

31542860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 20731733-T-G

http://identifiers.org/hco/18/GRCh38#31542862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20731735-A-C

31542862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20731735-A-G

31542862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20731735-A-T

http://identifiers.org/hco/18/GRCh38#31542872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20731742-A-C

31542872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20731742-A-G

31542872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20731742-A-T

31542873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20731743-T-G

31542951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20731815-G-A

31542951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20731815-G-C

31542951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20731815-G-T

31542970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20731834-T-C

31543113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20731965-T-G

31543118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20731970-G-A

31543118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20731970-G-T

http://identifiers.org/hco/18/GRCh38#31543129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20731982-C-A

http://identifiers.org/hco/18/GRCh38#31543137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20731990-C-A

http://identifiers.org/hco/18/GRCh38#31543141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20731994-A-C

31543141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20731994-A-G

31543141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20731994-A-T

31543154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20732007-A-G

31543168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20732025-T-C

31543235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20732088-A-G

31543235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20732088-A-T

31545403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20734058-A-G

31545789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20734438-G-T

31545816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20734465-T-C

31545817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20734466-A-G

31545828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20734477-C-T

31545906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 20734555-C-T

31545925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20734574-A-G

31545999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20734648-T-C

http://identifiers.org/hco/18/GRCh38#31546029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20734678-C-A

31546029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20734678-C-G

31546029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20734678-C-T

31546299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20734945-T-G

31546375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20735021-G-C

31546375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20735021-G-T

31546377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20735023-T-A

31546380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20735026-A-G

31546486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20735132-G-T

31546522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20735171-G-A

31546565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20735214-G-C

31546614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20735263-G-A

31546753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20735402-A-G

31546754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20735403-G-A

http://identifiers.org/hco/18/GRCh38#31546878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20735503-C-A

31546916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20735541-G-A

31546974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20735601-G-A

31546980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20735607-T-C

31546989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20735616-G-A

31546989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20735616-G-T

31547117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20735719-T-C

http://identifiers.org/hco/18/GRCh38#31547314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20735984-A-C

31547314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20735984-A-G

31547325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20735995-G-A

31547325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20735995-G-T

http://identifiers.org/hco/18/GRCh38#31547458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20736064-A-C

31547458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736064-A-G

31547472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736078-T-A

31547512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736103-A-G

http://identifiers.org/hco/18/GRCh38#31547525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20736116-A-C

31547535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736126-G-A

31547602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736180-G-A

31547602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736180-G-C

31547602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736180-G-T

31547603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736185-G-T

31547604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736186-G-A

31547604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736186-G-C

31547604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736186-G-T

31547621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736200-G-A

http://identifiers.org/hco/18/GRCh38#31547643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20736222-C-A

31547643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736222-C-G

31547643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736222-C-T

31547656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736230-A-G

31547656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736230-A-T

31548001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736709-C-G

31548001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736709-C-T

31548045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736747-G-A

31548078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20736781-T-C

31548363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20737063-G-A

31548439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20737149-A-T

31548596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20737306-A-G

31548692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20737429-G-A

31548724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20737459-C-T

31548931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3049
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20737654-G-T