219512471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75425210-A-T

219512529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75425288-G-C

219512578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75425344-G-A

219512793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75425570-T-C

http://identifiers.org/hco/2/GRCh38#219513037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#75425816-C-A

219513037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75425816-C-T

219513653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75426403-A-G

219513656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75426406-C-T

219514077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75426812-T-A

219514077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75426812-T-C

219514077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75426812-T-G

219514146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75426880-G-A

219514284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75427034-G-A

219514284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75427034-G-T

219514290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75427040-G-A

219514290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75427040-G-T

219514712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75427463-C-T

219514991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75427742-C-T

219515063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75427814-G-A

219515063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75427814-G-C

219515063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75427814-G-T

219515094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75427845-C-T

http://identifiers.org/hco/2/GRCh38#219515321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75428072-C-A

219515321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75428072-C-T

219515355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75428107-G-T

219515379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75428124-G-T

219515390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75428135-G-A

219515390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75428135-G-T

http://identifiers.org/hco/2/GRCh38#219515419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75428164-A-C

219515419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75428164-A-G

219515419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75428164-A-T

219516178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75428952-C-T

http://identifiers.org/hco/2/GRCh38#219516550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75429286-C-A

219516560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75429296-G-A

219516560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75429296-G-T

219516624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75429359-A-G

219516632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75429367-C-T

http://identifiers.org/hco/2/GRCh38#219516706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75429454-A-C

219516706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75429454-A-G

219516799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75429546-A-G

219516799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75429546-A-T

219516856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75429619-T-A

219516856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75429619-T-C

219516996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75429751-T-C

http://identifiers.org/hco/2/GRCh38#219517251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75430002-A-C

219517355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75430170-A-G

219517358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75430173-A-G

219517689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75430454-G-A

http://identifiers.org/hco/2/GRCh38#219518038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75430813-A-C

219518038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75430813-A-G

219518055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75430907-C-T

219518338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75431185-C-T

219518562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75431403-C-T

219518602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75431443-G-C

219518852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75431744-G-T

219519286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75431876-G-A

219519410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75431999-T-A

219519859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75432386-A-T

219520119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75432642-C-T

219520324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75432845-C-T

http://identifiers.org/hco/2/GRCh38#219520587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75433095-C-A

219520709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75433222-C-T

219520809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75433310-G-A

219520822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75433322-A-G

219521025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75433479-C-T

219521171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75433624-G-T

219521221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75433672-A-G

219521407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75433832-C-T

219521499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75433917-G-A

219521968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75434330-G-T

219522063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75434426-T-C

219522094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75434492-C-T

219522108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75434506-C-T

219522435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75434834-G-C

219522457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75434856-G-T

219522604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75435006-G-A

219522720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75435142-C-T

219522754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75435184-G-A

219522754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75435184-G-C

219522754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75435184-G-T

219522981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75435403-T-A

219523107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75435569-C-T

219523137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75435608-C-T

219523184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75435665-G-T

219523390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75435869-C-T

219524706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75437108-C-T

219524941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75439439-T-A

219524941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75439439-T-C

219525155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75439687-G-A

219525285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75439871-C-G

219525451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75440030-C-G

219525619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75440233-G-A

219525641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75440249-C-T

219525692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75440287-T-C

http://identifiers.org/hco/2/GRCh38#219525793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75440385-C-A

219526127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75440772-C-T

http://identifiers.org/hco/2/GRCh38#219526128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#75440773-A-C

219526268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75440917-G-A

219526418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75441022-G-A

219526618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75441224-G-A

219527458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75441962-G-A

219527640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75442139-G-A

219527652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75442151-C-G

219527660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75442159-C-T

http://identifiers.org/hco/2/GRCh38#219527783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75442278-C-A

219527803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75442481-C-T

219527901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75442549-C-G

219527936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75442583-C-G

219527936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75442583-C-T

219528044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75442648-C-T

219528143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75442747-A-G

219528336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75442853-A-G

219528647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75442994-C-T

219528959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443151-C-T

219529037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443254-C-G

219529046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443263-G-T

219529213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443420-C-T

219529547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443666-G-A

219529589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443696-C-T

219529592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443699-G-A

219529662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443751-T-C

219529779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443879-T-G

219529851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443951-G-T

219529941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75444051-C-T

219529966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75444076-G-C

219530004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75444111-C-T

219530235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75444326-A-T

219530248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75444339-C-T

219530314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75444410-G-A

219530314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75444410-G-C

219530365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75444461-G-T

219530463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75444545-G-C

219530514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75444596-A-G

219530519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75444601-C-T

219530881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75444854-G-T

219531384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75445367-A-G

219531417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75445392-G-A

219531452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75445427-G-A

219531452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75445427-G-C

219531452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75445427-G-T

219531496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75445473-G-C

219531496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75445473-G-T

219531510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75445490-G-C

219532056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75446056-G-A

219532056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75446056-G-C

219532056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75446056-G-T

219532080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75446080-C-T

219532089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75446089-C-T

219532522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75446517-G-T

http://identifiers.org/hco/2/GRCh38#219532541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75446536-C-A

219532609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75446583-G-A

219532609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75446583-G-C

219532702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75446696-G-A

219532702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75446696-G-T

http://identifiers.org/hco/2/GRCh38#219532713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75446750-C-A

219532713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75446750-C-T

219532752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75446789-T-C

219532752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75446789-T-G

219532824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75446863-G-A

http://identifiers.org/hco/2/GRCh38#219533024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75447060-C-A

219533046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75447081-G-A

219533046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75447081-G-T

219533129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75447163-G-A

219533129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75447163-G-T

219533143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75447177-G-A

219533143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75447177-G-T

219533145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75447179-A-G

219533318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75447377-A-G

http://identifiers.org/hco/2/GRCh38#219533358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75447425-C-A

219533358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75447425-C-T

http://identifiers.org/hco/2/GRCh38#219533381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75447472-C-A

219533381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75447472-C-G

219533381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75447472-C-T

219533413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75447504-G-C

219533444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75447530-C-G

219533444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75447530-C-T

219533650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75447725-G-A

http://identifiers.org/hco/2/GRCh38#219533696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75447772-C-A

219533696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75447772-C-T

http://identifiers.org/hco/2/GRCh38#219534696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75448551-A-C

http://identifiers.org/hco/2/GRCh38#219535021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75448798-C-A

219535021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75448798-C-G

219535021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75448798-C-T

219535061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75448828-G-T

219535063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75448830-G-A

219535063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75448830-G-T

219535102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75448867-T-A

219535102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75448867-T-C

http://identifiers.org/hco/2/GRCh38#219535117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75448882-C-A

219535117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75448882-C-T

219535217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75448974-C-T

219535235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 75448992-T-G

http://identifiers.org/hco/2/GRCh38#219537016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75449421-C-A

219537016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75449421-C-T

http://identifiers.org/hco/2/GRCh38#219537047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75449450-C-A

219537128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75449528-G-A

219537128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75449528-G-C

219537128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75449528-G-T

http://identifiers.org/hco/2/GRCh38#219537365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75449722-C-A

219537365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75449722-C-T

219537399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75449738-G-C

http://identifiers.org/hco/2/GRCh38#219537406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75449745-C-A

http://identifiers.org/hco/2/GRCh38#219537544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75449844-C-A

219537544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75449844-C-G

219537544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75449844-C-T

219537549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75449849-G-T

http://identifiers.org/hco/2/GRCh38#219537586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75449865-A-C

219537586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75449865-A-G

http://identifiers.org/hco/2/GRCh38#219537587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75449866-C-A

219537587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75449866-C-G

219537587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75449866-C-T

219537727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75449982-G-A

219537754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75450009-A-T

219537954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 75450184-C-T

219538007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75450237-C-T

219538047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75450277-G-A

219538151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75450403-G-T

219538216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75450460-C-T

219538228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75450472-C-T

219538250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75450494-G-T

219538310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75450549-A-G

219538310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75450549-A-T

219538311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75450550-G-A

219538311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75450550-G-C

219538311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75450550-G-T

219538426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75450643-G-T

http://identifiers.org/hco/2/GRCh38#219538658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75450864-C-A

http://identifiers.org/hco/2/GRCh38#219538704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75450916-C-A

219538704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75450916-C-T

http://identifiers.org/hco/2/GRCh38#219538713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75450925-C-A

219538723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21263
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75450935-T-C