75292059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79708657-A-G

75292096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79708688-A-G

75292398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79709012-G-T

75292437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79709052-G-A

75292437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79709052-G-T

75292442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79709057-G-T

75292985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79709542-A-G

75293222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79710064-C-T

75293289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79710130-T-C

75293306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79710147-G-A

75293315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79710156-G-A

http://identifiers.org/hco/6/GRCh38#75293317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79710158-C-A

http://identifiers.org/hco/6/GRCh38#75293387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79710224-C-A

75293463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79710249-T-C

75293463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79710249-T-G

75293576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79710335-C-T

75293651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79710407-C-T

75293796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79710464-G-T

http://identifiers.org/hco/6/GRCh38#75293834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79710492-A-C

75293834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79710492-A-G

75293834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79710492-A-T

75293876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79710510-T-C

http://identifiers.org/hco/6/GRCh38#75293877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79710511-C-A

75294111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79710785-C-T

75294130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79710802-C-T

75294204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79710868-G-A

75294263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79710919-G-T

75294368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79711026-G-A

http://identifiers.org/hco/6/GRCh38#75294434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79711087-C-A

75294434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79711087-C-T

75294536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79711163-G-T

75294552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79711179-G-C

75294932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79711481-T-A

75294932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79711481-T-G

75294935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79711484-G-T

75295441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79711860-A-G

75295441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79711860-A-T

75295533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79711945-G-A

75295533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79711945-G-T

75295571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79711983-A-G

75295741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79712153-G-T

75295786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79712383-G-T

75295834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79712430-G-T

75295909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79712458-T-C

75295945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79712494-T-C

http://identifiers.org/hco/6/GRCh38#75296049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79712609-C-A

75296049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79712609-C-G

75296069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79712625-A-G

75296245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79712818-A-G

http://identifiers.org/hco/6/GRCh38#75296249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79712822-C-A

75296249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79712822-C-G

75296371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79713065-G-A

75296371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79713065-G-C

75296517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79713274-T-A

75296592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79713339-C-G

75296592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79713339-C-T

http://identifiers.org/hco/6/GRCh38#75296625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79713371-C-A

75296625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79713371-C-G

http://identifiers.org/hco/6/GRCh38#75296648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79713393-C-A

75296648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79713393-C-T

75296690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79713469-G-T

http://identifiers.org/hco/6/GRCh38#75296704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79713530-C-A

75296704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79713530-C-T

75296884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79713700-A-G

75296901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79713717-T-A

http://identifiers.org/hco/6/GRCh38#75296909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79713725-C-A

75296964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79713791-G-A

75296986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79713811-G-T

75297011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79713830-G-T

75297290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79714127-T-C

75297671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79714465-T-A

75297702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79714493-A-G

75297719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79714514-A-T

75297819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79714622-G-C

75297819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79714622-G-T

75297935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79714739-T-A

75298040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79714805-C-T

75298211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79714946-T-C

75298544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79715097-A-G

75298998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79715426-T-A

75299021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79715449-A-T

75299066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79715468-T-G

http://identifiers.org/hco/6/GRCh38#75299274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79715603-A-C

http://identifiers.org/hco/6/GRCh38#75299431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79715721-C-A

75299688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79715959-T-G

http://identifiers.org/hco/6/GRCh38#75300183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79716436-A-C

75300205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79716458-A-T

75300210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79716463-C-T

75300226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79716479-T-C

75300397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79716636-G-A

75301089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79717253-T-C

http://identifiers.org/hco/6/GRCh38#75303710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79718355-C-A

75303743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79718430-G-A

75303787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79718479-A-T

75303924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79718744-G-A

75304125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79718960-C-T

75305283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79719904-A-G

75305399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720005-C-G

http://identifiers.org/hco/6/GRCh38#75305671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79720235-C-A

75305686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720250-G-A

http://identifiers.org/hco/6/GRCh38#75305777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79720340-C-A

75305798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720361-G-T

http://identifiers.org/hco/6/GRCh38#75305815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79720378-C-A

75305815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720378-C-G

75305822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720385-T-A

75305822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720385-T-C

75305822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720385-T-G

75305836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720401-T-G

75305923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720478-A-G

75305978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720531-A-G

75306155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720795-T-C

75306165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720805-T-G

75306360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79721000-A-G

75306474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79721100-A-G

http://identifiers.org/hco/6/GRCh38#75306493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79721119-A-C

75306493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79721119-A-G

75306520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79721147-A-T

75307127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79721383-C-T

75307942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79722194-A-G

75307942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79722194-A-T

75308352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79722592-G-A

75308366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79722606-G-A

75308366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79722606-G-C

http://identifiers.org/hco/6/GRCh38#75308515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79722790-C-A

75308518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79722793-G-A

75308518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79722793-G-T

75308934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79723212-T-C

http://identifiers.org/hco/6/GRCh38#75308957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79723234-C-A

http://identifiers.org/hco/6/GRCh38#75309019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79723296-C-A

75309024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79723301-A-G

75309047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79723322-G-T

75309265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79723455-T-C

75309387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79723574-G-C

75309524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79723703-T-G

http://identifiers.org/hco/6/GRCh38#75309573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79723751-C-A

75311841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79724120-C-T

http://identifiers.org/hco/6/GRCh38#75312001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79724267-C-A

75312143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79724392-A-G

http://identifiers.org/hco/6/GRCh38#75312352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79725140-C-A

75312352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79725140-C-T

75312555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 79725338-G-A

75312555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79725338-G-C

http://identifiers.org/hco/6/GRCh38#75312559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79725342-A-C

75312559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79725342-A-G

75312712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79725498-G-A

75312712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79725498-G-T

75312715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79725501-G-A

75312790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79725576-T-C

75313042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79725828-C-T

75313198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79725984-G-A

75313363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79726149-G-T

75313366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79726152-T-A

75313399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79726185-G-A

75313399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79726185-G-T

75313417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79726203-G-C

http://identifiers.org/hco/6/GRCh38#75313516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79726302-C-A

75313636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79726422-G-A

75313636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79726422-G-C

75313636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79726422-G-T

http://identifiers.org/hco/6/GRCh38#75313700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79726486-C-A

75313700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79726486-C-T

75314215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79727001-T-C

75314260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79727046-T-G

75314773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79727559-C-T

75315004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79727790-C-T

75315216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79728002-T-C

75315284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79728115-G-A

75315284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79728115-G-C

75315284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79728115-G-T

75315304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79728141-A-T

75315351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79728211-G-T

75315479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79728325-C-T

http://identifiers.org/hco/6/GRCh38#75315855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79728643-A-C

75315863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79728649-C-T

http://identifiers.org/hco/6/GRCh38#75316015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79728980-A-C

75316039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79729004-A-T

75316301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79729482-G-A

75316780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79729831-C-G

75316780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79729831-C-T

75323541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79729998-T-A

75323572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79730036-G-T

75326698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79730624-T-G

75326929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79730858-T-C

75326988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79730919-G-A

75327453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79731347-T-C

75327488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79731382-G-A

75327492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79731386-A-G

75327936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79731801-C-T

75327988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79731850-C-T

75328259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79732136-G-C

http://identifiers.org/hco/6/GRCh38#75328319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79732197-A-C

75328503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79732340-G-C

75329061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79732545-G-T

75329062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79732546-A-T

75329081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79732565-T-C

75329092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79732576-T-A

75329092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79732576-T-C

75329166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79732629-T-C

75329196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79732658-T-G

75329199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79732661-A-G

75329405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79732801-C-T

75329406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79732802-A-G

http://identifiers.org/hco/6/GRCh38#75329584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79732970-A-C

75330123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79733304-G-A

75330175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79733325-A-G

75330615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79733951-G-C

75332323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79735580-T-C

75332365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79735622-T-C

75332437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79735685-C-G

75332499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79735751-C-T

75332556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79735808-C-G

75332577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79735829-G-A

75332637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79736483-T-C

75332860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79736653-T-C

75332867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79736663-C-T

75332915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79736711-A-G

75333308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79737088-A-G

75333637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79737202-T-C

75333888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79737435-C-G

75334385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79737903-T-A

75334385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79737903-T-C

http://identifiers.org/hco/6/GRCh38#75334441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79737956-C-A

75334626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79738140-G-T

75334735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79738235-G-C

75334735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79738235-G-T

75334759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79738259-C-T

75334784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79738285-G-C

75334818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79738319-T-C

75334833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79738334-A-G

75335454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79739774-T-A

75335454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79739774-T-C

75335536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79739857-T-C

75335765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79740042-A-G

75336134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79740475-G-C

http://identifiers.org/hco/6/GRCh38#75336164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79740502-C-A

75336171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79740509-C-G

75336299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79740623-C-T

75336539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79740847-G-A

75337194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79744370-T-C

75337327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79744460-G-T

75337628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79744710-T-C

75337630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79744712-G-A

75337776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79744856-T-C

75337776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79744856-T-G

75337874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79744937-A-G

75337962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79745005-T-C

75337962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79745005-T-G

75338246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79750193-G-T

75338259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79750206-C-T

http://identifiers.org/hco/6/GRCh38#75338324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79750271-A-C

75338724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79750659-C-G

75338724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79750659-C-T

75338947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79750856-A-G

75338947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79750856-A-T

75339160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79751048-A-G

75339275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79751144-T-C

http://identifiers.org/hco/6/GRCh38#75339398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79751259-A-C

75339570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79751426-T-C

75339621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79751460-A-G

75347052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79754361-G-A

75347135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79754480-A-G

75347146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79754491-A-G

75347299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79754616-T-C

75347402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79754703-A-G

75347905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79755534-G-A

75347973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79755593-T-C

75347992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79755613-A-G

75348034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79755664-T-A

75348222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79755789-G-A

75348305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79755874-A-G

75348332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79755906-G-C

75348414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79755982-C-T

75348472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79756036-T-C

75348478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79756042-A-G

75348641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79756204-T-A

75348867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79756415-G-A

75348867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79756415-G-T

75348954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79756500-G-A

75349290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79756758-C-T

75351859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79758013-T-C

75351890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79758041-A-T

75352468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79759417-A-G

75352468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79759417-A-T

75352476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79759425-G-C

75352572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79759541-G-A

75352797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79760337-A-G

75352906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79760374-A-G

http://identifiers.org/hco/6/GRCh38#75352937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79760344-C-A

http://identifiers.org/hco/6/GRCh38#75352944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79760337-C-A

75352944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79760337-C-T

75353534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79760899-A-G

75353534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79760899-A-T

75353613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: synonymous variant
orthologous variants: 79760978-G-A

75353613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: missense variant
orthologous variants: 79760978-G-T

75353631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: synonymous variant
orthologous variants: 79760996-G-A

75353631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: synonymous variant
orthologous variants: 79760996-G-T

75353780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79761141-A-G

75353787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79761148-G-T

75353807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79761168-T-A

75353807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79761168-T-G

75353808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79761169-T-A

75353808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79761169-T-C

75353815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79761176-A-G

75354943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79761845-A-G

75357085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79762525-G-A

75357134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79762573-G-A

75357134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79762573-G-T

75357159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79762599-T-C

75357185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron variant
orthologous variants: 79762625-A-G

http://identifiers.org/hco/6/GRCh38#75357261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79762696-C-A

http://identifiers.org/hco/6/GRCh38#75357872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79763203-A-C

75357990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79763306-T-C

75358357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79763987-A-T

75358359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79763989-A-G

75358516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79764133-C-T

http://identifiers.org/hco/6/GRCh38#75358548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79764162-C-A

75359502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79764472-G-T

75359669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79764647-C-T

75359746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79764711-G-A

75359746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79764711-G-C

75360450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79765196-T-A

75360450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79765196-T-C

75360711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79764965-T-C

75361480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79766090-A-G

75361490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79766100-T-A

75361587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79766200-T-C

http://identifiers.org/hco/6/GRCh38#75361821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79766430-C-A

75361821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79766430-C-T

75361865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79766484-T-C

75361899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79766504-A-T

75361924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79766529-G-C

75361924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79766529-G-T

75362107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79766671-T-C

75362481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79767066-T-C

75362692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79767267-G-A

75362694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79767269-T-C

75362729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79767349-G-A

75362729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79767349-G-C

75362729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79767349-G-T

75362807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79767425-T-G

75362813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79767431-C-G

75362876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79767494-G-C

75362876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79767494-G-T

75362950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79767568-T-C

75362953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79767571-C-T

75362969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79767576-C-G

http://identifiers.org/hco/6/GRCh38#75363005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79767612-C-A

75363005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79767612-C-T

http://identifiers.org/hco/6/GRCh38#75363009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79767616-C-A

75363009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79767616-C-T

75363059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79767665-T-A

http://identifiers.org/hco/6/GRCh38#75363095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79767701-C-A

75363095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79767701-C-T

75363309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79767889-T-C

75363437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79768031-A-T

75363442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79768036-T-C

75363761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79768303-C-T

75363845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79768358-A-G

75363910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79768420-G-A

http://identifiers.org/hco/6/GRCh38#75363923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79768433-C-A

75363937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79768447-C-G

http://identifiers.org/hco/6/GRCh38#75363965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79768472-A-C

75363985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79768492-A-G

75364131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79768677-T-G

75365999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79769984-C-G

75366038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79770023-A-G

75366038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79770023-A-T

75366043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79770026-T-C

75366108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79770082-G-A

75366223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79770187-T-C

75367300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79772467-T-C

http://identifiers.org/hco/6/GRCh38#75367723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79772951-C-A

75367723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79772951-C-T

75368209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79773415-C-G

75368209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79773415-C-T

75368450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79773666-T-C

75368526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79773730-G-A

75368570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79773763-G-A

75369126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79775671-T-C

75369181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79775728-G-T

75369249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79775781-G-A

75369270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79775802-G-A

75369370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79775919-T-C

75369691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79776251-G-A

75369698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79776257-G-C

75369749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79776306-G-A

75369749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79776306-G-T

75369878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79776568-G-A

75370366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79777019-C-T

75370422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79777075-G-A

75370448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79777097-C-T

http://identifiers.org/hco/6/GRCh38#75373078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79778681-A-C

75373217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79778822-A-G

75373277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79778878-G-C

75373424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79779024-A-G

75374151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79779530-A-G

75374304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79779633-A-G

http://identifiers.org/hco/6/GRCh38#75374771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79779759-A-C

75375176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79780148-G-A

75375220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79780193-G-T

75375229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79780202-G-C

75375414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79780361-G-A

75375673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79780584-A-G

75375707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79780636-A-G

75375937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79780877-T-A

75375937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79780877-T-C

75376492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79781251-G-A

75376492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79781251-G-C

75376492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79781251-G-T

75376813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79781607-G-A

http://identifiers.org/hco/6/GRCh38#75376890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79781875-A-C

75376972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79781956-T-G

75377035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79782010-C-T

75381572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79782484-G-T

75381660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79782565-G-A

75382456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79783310-G-A

75382596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79783449-T-A

75382657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79783510-G-A

75382999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79783849-T-C

75383006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79783856-G-C

75383006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79783856-G-T

75383584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79785351-A-G

75383585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79785352-T-C

75383632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79785401-T-C

75383658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79785422-T-A

75383935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79785698-T-G

75384137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79786420-A-G

75384137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79786420-A-T

75384213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79786502-A-G

75385530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79786817-G-T

75385535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79786822-T-C

75385671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79786916-C-T

http://identifiers.org/hco/6/GRCh38#75385775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79787020-C-A

http://identifiers.org/hco/6/GRCh38#75386093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#79787329-C-A

http://identifiers.org/hco/6/GRCh38#75386243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#79787477-C-A

http://identifiers.org/hco/6/GRCh38#75386508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#79787734-C-A

75386642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79787849-C-T

75386647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79787854-G-T

75386671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79787876-C-T

75386719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79787924-C-T

75386768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79787978-G-C

http://identifiers.org/hco/6/GRCh38#75398245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#79793260-C-A

75398245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79793260-C-T

75398562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79793512-C-G

75398586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79793527-G-C

75398623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79793550-T-A

75398629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79793556-G-C

75398755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79793657-T-C

75398759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79793661-A-G

75399180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79794939-A-G

75399183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79794942-A-G

http://identifiers.org/hco/6/GRCh38#75401779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79797349-A-C

75402219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79797804-G-C

75402442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79798017-C-T

http://identifiers.org/hco/6/GRCh38#75402703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#79798278-A-C

75403102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79799065-T-C

75403164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79799126-G-C

75403998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79799670-A-T

75404322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79800013-C-G

75404475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79800162-T-C

75404782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79800469-G-T

http://identifiers.org/hco/6/GRCh38#75405297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79800956-C-A

75407795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79801760-C-T

75407850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79801814-T-A

75408097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79802061-A-T

75408164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79802133-T-C

75408276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79802231-G-A

75408857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79802396-C-T

75408934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79802475-C-T

75409056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79802599-T-C

http://identifiers.org/hco/6/GRCh38#75409271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79803000-C-A

75409271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79803000-C-G

75409301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79803014-A-G

http://identifiers.org/hco/6/GRCh38#75410123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79803075-C-A

75410166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79803116-C-G

75410166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79803116-C-T

75412693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79803649-G-A

75412834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79803765-T-C

75413005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79803948-C-G

75413320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79804234-C-T

75413388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79804303-G-A

75413438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79804350-G-A

75413543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79804438-G-T

75413597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79804491-G-A

75413916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79804759-A-G

75413996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79804827-A-G

75414204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805028-G-A

http://identifiers.org/hco/6/GRCh38#75414305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79805120-A-C

75414455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805248-T-C

75414560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805352-T-A

75414560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805352-T-C

75414578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805377-G-A

75414578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805377-G-T

75414582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805381-A-T

75414620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805416-G-C

75414620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805416-G-T

http://identifiers.org/hco/6/GRCh38#75414660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79805453-C-A

75414660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805453-C-T

75414661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805454-A-G

75414775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 79805555-T-A

75414775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79805555-T-C

75414787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79805567-A-G

http://identifiers.org/hco/6/GRCh38#75414811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79805591-A-C

75415008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805779-T-C

http://identifiers.org/hco/6/GRCh38#75415064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79805830-C-A

75415521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79806436-T-A

75415551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79806444-A-G

http://identifiers.org/hco/6/GRCh38#75415556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79806449-C-A

75415556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79806449-C-G

75415641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79806476-C-T

75415729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79806567-G-C

75415923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79806743-C-G

75415923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79806743-C-T

75416125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79818225-G-C

75416125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79818225-G-T

75416269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79818339-G-A

75416295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79818366-T-G

75416531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79818591-C-T

75416606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79818914-G-A

75416606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79818914-G-T

75416656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79819003-G-A

75416715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79819046-T-C

75416845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79819171-G-T

75417002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79819382-G-T

75417211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79819526-A-G

75417532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79819821-T-C

75417679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79819958-T-C

http://identifiers.org/hco/6/GRCh38#75418261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79820139-A-C

75418298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79820174-A-G

75418348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79820232-G-T

75418399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79820280-C-T

75418805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79820658-G-A

75418873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79820716-G-C

75419094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79820930-T-C

75419157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79821204-T-C

75419158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79821205-G-A

75419229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79821284-C-T

http://identifiers.org/hco/6/GRCh38#75419410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79821463-A-C

75419593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79821628-G-A

http://identifiers.org/hco/6/GRCh38#75419607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79821640-A-C

75419963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79822034-G-C

75420046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79822115-T-C

75420060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79822129-C-G

75420156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79822332-C-T

75420321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79822500-A-G

75420368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79822721-G-A

75420480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79822825-T-C

75420521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79822859-T-C

75420635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79822964-G-A

75422129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79824307-T-A

75422129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79824307-T-C

75422314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79824679-T-C

75424576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79825535-A-T

75424621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79825625-T-C

75425167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79826156-C-T

http://identifiers.org/hco/6/GRCh38#75425233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79826213-A-C

75425491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79826476-T-C

75425659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79826614-C-T

75425813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79826741-A-G

75426085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79826986-G-C

75426132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79827033-C-T

75426150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79827049-A-G

http://identifiers.org/hco/6/GRCh38#75426196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79827088-C-A

75426744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79827578-C-T

http://identifiers.org/hco/6/GRCh38#75427066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79828065-C-A

75427088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79828083-C-T

75427225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79828190-T-C

75430863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79829153-G-T

75431048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79829313-C-G

75431448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79829675-G-A

75431504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79829726-A-G

75431596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79829815-G-C

75431768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79829979-C-T

75431819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79830023-T-G

75431895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79830108-T-C

75431937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79830152-T-C

75431995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79830204-A-G

75432075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79830283-C-T

75432133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79830449-G-C

75432191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79830590-G-T

75432349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79830725-G-A

75432449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79830817-T-C

75435406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79831477-T-C

75435581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79831792-A-G

75435642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79831849-A-G

75437156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79833438-C-T

75437407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79833727-T-C

75437562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79833882-T-C

75438001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79834289-C-T

75438134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79834426-G-A

75438479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79834764-T-C

75438482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79834767-C-T

75438486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79834771-G-A

75438486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79834771-G-C

75438740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835034-A-T

http://identifiers.org/hco/6/GRCh38#75438780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79835074-C-A

75438864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835437-T-C

75438939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835507-G-A

75439708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835734-G-A

75445438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79841208-C-G

75446284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79841970-G-T

75446388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79842071-T-A

75446557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79842233-T-C

75446835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79842502-T-C

75447156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79842820-T-G

http://identifiers.org/hco/6/GRCh38#75447382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79843195-C-A

75447677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79843476-T-A

75447741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79843574-T-C

75447942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79843732-G-A

75447989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79843773-G-C

75448022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79843789-C-T

75448178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79843943-C-T

75448214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79843973-A-G

75448240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79843998-T-A

75448283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79844038-C-T

75448299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79844053-T-C

75448319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79844072-T-C

75449681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79844556-T-C

75449698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79844573-A-G

75449842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79844698-G-A

75454904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79844979-C-T

75455118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845180-G-A

75455118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845180-G-C

75455118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845180-G-T

http://identifiers.org/hco/6/GRCh38#75455157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79845215-C-A

75455157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845215-C-T

http://identifiers.org/hco/6/GRCh38#75455180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79845238-C-A

75455180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79845238-C-T

http://identifiers.org/hco/6/GRCh38#75455191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79845247-C-A

http://identifiers.org/hco/6/GRCh38#75455219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79845274-C-A

75455219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79845274-C-T

75455257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79845310-G-T

75455381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845428-G-A

75455381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845428-G-C

75455390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845437-A-G

75455390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845437-A-T

75455491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845537-T-C

75455558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845604-A-G

75455580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845628-A-G

75455591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845639-C-T

http://identifiers.org/hco/6/GRCh38#75455676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79845712-C-A

75455676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845712-C-G

75455758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845795-T-C

75455808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845845-C-T

75455896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79846397-C-G

http://identifiers.org/hco/6/GRCh38#75458384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79850734-C-A

75458599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79850993-T-G

75458736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79851133-G-T

http://identifiers.org/hco/6/GRCh38#75458849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79851245-C-A

75458859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79851255-G-T

75458911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851287-C-T

http://identifiers.org/hco/6/GRCh38#75458912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79851288-C-A

75459041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851422-A-G

75459045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851426-G-A

75459045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851426-G-T

75459232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851611-A-T

75459282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851658-G-A

75459324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851697-A-T

75459452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851823-G-T

75459711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852093-A-T

75459775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852155-T-C

75459864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852240-C-G

75459864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852240-C-T

75459960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852337-G-T

75460061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852417-T-A

75460061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852417-T-C

75461533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852737-T-C

75461661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852846-G-A

75461682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852867-A-T

75461862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79853043-T-C

75462202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79853451-C-T

75462384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79853594-G-A

75462942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79854974-G-A

75463164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79855399-A-G

75463471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79856858-A-G

75463587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79856958-G-T

75463591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79856962-T-A

75463629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79856985-G-A

75463761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79857090-C-T

75463906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79857229-G-A

75464199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79857546-T-A

75464199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79857546-T-C

75464495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79857710-T-G

75464589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79857804-T-C

75464711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79857924-A-T

75464797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79858001-C-T

75464820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79858023-C-T

75464827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79858042-G-T

75464932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79858111-T-C

75464945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79858123-A-G

http://identifiers.org/hco/6/GRCh38#75464954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79858132-C-A

http://identifiers.org/hco/6/GRCh38#75464975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79858153-C-A

75464975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79858153-C-T

75465015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79858194-A-G

http://identifiers.org/hco/6/GRCh38#75472084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79861454-C-A

75472094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79861468-T-C

75472221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79861594-A-G

http://identifiers.org/hco/6/GRCh38#75472513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79861867-A-C

75472912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79862246-A-G

75476881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79867391-T-G

75477043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79867545-T-C

75477059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79867564-T-A

75477084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79867762-C-T

75477153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79867835-C-G

75477153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79867835-C-T

75477679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79867911-T-C

75477763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79868034-G-A

http://identifiers.org/hco/6/GRCh38#75478230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79869242-C-A

75478230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79869242-C-T

75478312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79869320-G-A

75478415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79869401-C-T

75479410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79870000-G-A

75480090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79870740-T-G

75480112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79870776-T-C

75480708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79871376-T-C

http://identifiers.org/hco/6/GRCh38#75480990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79871648-A-C

75481405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79872310-T-C

75481450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79872351-C-T

75482103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79872925-C-T

75482198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79873019-T-C

http://identifiers.org/hco/6/GRCh38#75482254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79873084-C-A

75482268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79873098-T-A

75482309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79873139-A-G

75482447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79873275-G-A

75482447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79873275-G-C

75482546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79873417-A-G

75482588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79873445-A-G

75482627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79873483-T-C

http://identifiers.org/hco/6/GRCh38#75483169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79873979-A-C

75483261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79874091-G-A

http://identifiers.org/hco/6/GRCh38#75483415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79874242-A-C

75483480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79874305-G-A

75483621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79874431-T-C

75483705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79874513-T-G

75484234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79875017-C-T

http://identifiers.org/hco/6/GRCh38#75484236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79875019-A-C

75484711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79875652-A-G

75484738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79875679-G-A

75485397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79876304-T-C

75485397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79876304-T-G

75485611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79876746-G-A

http://identifiers.org/hco/6/GRCh38#75485697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79876832-A-C

http://identifiers.org/hco/6/GRCh38#75486290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79877141-A-C

75486298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79877149-C-T

http://identifiers.org/hco/6/GRCh38#75486358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79877219-A-C

75486440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79877292-T-C

75486449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79877293-A-G

75486488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79877332-A-G

75486504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79877347-C-T

75486674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79877518-C-T

75486807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79877716-G-A

75487085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79878048-G-A

75487349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79878292-C-T

75487366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79878309-A-G

75487579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79878508-A-T

75487808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79878735-C-T

75487815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79878742-A-G

75487861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79878787-G-A

75488331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79879242-G-A

75488331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79879242-G-C

75488410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79879320-T-A

75488410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79879320-T-C

75488739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79879630-T-C

75488926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79879813-C-T

75489098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79879979-T-C

75489484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79880359-T-C

75489681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79880545-C-T

75489821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79880681-T-C

75490068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79881313-T-C

75490090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79881335-A-G

http://identifiers.org/hco/6/GRCh38#75490182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79881433-C-A

75490182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79881433-C-T

75490943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79882055-T-C

75490948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79882060-A-G

http://identifiers.org/hco/6/GRCh38#75491212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79882272-C-A

75491268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79882325-G-A

75491448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79882511-A-T

75491595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79882626-G-A

75491595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79882626-G-C

75491595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79882626-G-T

75491605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79882636-C-T

75491720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79882753-A-G

75491771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79882801-A-G

75491904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79882929-A-G

75492016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79883025-T-G

http://identifiers.org/hco/6/GRCh38#75492972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79884322-C-A

75493373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79884687-T-C

http://identifiers.org/hco/6/GRCh38#75493756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21015
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79885065-C-A