221418677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77344468-A-G

221418769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77344559-G-A

221418769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77344559-G-T

221419061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77344870-C-T

http://identifiers.org/hco/2/GRCh38#221419142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77344951-A-C

221419201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77345010-T-C

221419243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77345052-A-G

221419455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77345269-C-T

221419586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77345398-T-A

http://identifiers.org/hco/2/GRCh38#221419938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77345682-C-A

221419938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77345682-C-T

221419949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77345710-A-G

221419954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77345715-G-T

221419955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77345716-G-A

221419955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77345716-G-C

221419955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77345716-G-T

http://identifiers.org/hco/2/GRCh38#221420179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77345948-C-A

221420179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77345948-C-G

221420179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77345948-C-T

221420204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77345973-C-T

http://identifiers.org/hco/2/GRCh38#221420282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77346052-C-A

221420282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77346052-C-T

221420356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77346117-A-G

http://identifiers.org/hco/2/GRCh38#221421966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77346697-C-A

221421966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77346697-C-T

http://identifiers.org/hco/2/GRCh38#221422055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77346807-A-C

221422074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77346826-T-A

221422074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77346826-T-C

221422201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77346907-A-G

221422349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77347054-C-T

221422415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77347101-G-A

221422648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77347253-A-G

221422695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77347285-A-G

221423118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77347561-G-A

221423214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77347642-T-C

221423326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77347753-C-T

221423604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348003-A-T

http://identifiers.org/hco/2/GRCh38#221423626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77348025-C-A

221424143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348442-T-A

221424158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348460-G-C

http://identifiers.org/hco/2/GRCh38#221424182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77348522-C-A

221424182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348522-C-G

221424411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348747-C-T

221424501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348854-T-A

221424501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348854-T-C

221424527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348876-T-C

221424659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77349029-G-A

221425097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77349404-T-A

221425097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77349404-T-C

221425159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77349473-C-T

221425240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77349579-G-A

221425242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77349581-G-A

221425242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77349581-G-T

221425406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77349747-T-C

http://identifiers.org/hco/2/GRCh38#221425467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77349808-C-A

221425477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77349818-G-T

221425482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77349823-C-T

221425578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3 prime UTR variant
orthologous variants: 77349913-T-G

221425660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3 prime UTR variant
orthologous variants: 77349998-G-T

221425686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3 prime UTR variant
orthologous variants: 77350024-G-A

221425686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3 prime UTR variant
orthologous variants: 77350024-G-C

http://identifiers.org/hco/2/GRCh38#221425688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77350026-A-C

221425723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3 prime UTR variant
orthologous variants: 77350056-G-A

221425723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3 prime UTR variant
orthologous variants: 77350056-G-T

221425741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 3 prime UTR variant
orthologous variants: 77350074-A-G

221426303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77350641-G-T

221426339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77350677-A-T

221426356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77350694-T-C

221426367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77351309-T-G

221426370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77351312-T-A

221426381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77351325-G-A

221426381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77351325-G-T

221426709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77351597-G-A

221426709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77351597-G-T

http://identifiers.org/hco/2/GRCh38#221426743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77351625-C-A

221426858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77351726-G-A

221427054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77351920-C-G

221427054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77351920-C-T

221427149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77352018-C-G

221427413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77352259-A-T

221427603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77352426-G-A

221427603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77352426-G-C

221428104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77352897-A-G

221428466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77353230-T-A

http://identifiers.org/hco/2/GRCh38#221429833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77353928-C-A

221429833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77353928-C-T

221429846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77353941-G-A

221429846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77353941-G-C

221429915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77354009-A-G

221430050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 77354143-G-A

221430050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 77354143-G-T

221430124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 77354217-G-A

221430137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 77354230-A-G

221430636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77354626-T-C

221430655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77354644-C-T

221430934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77354868-A-T

221431076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77355122-A-T

221431329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77355365-G-T

221431488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77355515-C-G

221431516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77355545-G-A

221431605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77355640-G-C

221431739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77355772-A-G

221432050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77356052-G-T

221432201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77356127-T-C

221432318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77356219-C-T

221432572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77356468-T-G

221433247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77356656-A-G

221433248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77356657-C-T

221433733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77357181-C-T

http://identifiers.org/hco/2/GRCh38#221433812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77357262-C-A

221433936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77357312-T-C

221433939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77357315-T-C

221433939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77357315-T-G

221434073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77357454-A-G

221434316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77357676-A-T

221434361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77357725-A-G

221434378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77357741-C-G

221434378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77357741-C-T

http://identifiers.org/hco/2/GRCh38#221434420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77357781-C-A

221434420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77357781-C-G

221434420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77357781-C-T

221435419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77358713-A-G

221436230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77359328-C-T

221436322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77359425-A-G

221436339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77359442-G-A

221436339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77359442-G-T

221436340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77359443-T-G

221436385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77359492-C-G

221436385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77359492-C-T

http://identifiers.org/hco/2/GRCh38#221436386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77359493-C-A

221436386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77359493-C-G

221436386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77359493-C-T

http://identifiers.org/hco/2/GRCh38#221436390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77359497-C-A

221436684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77359790-A-G

221436707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77359813-G-A

221436707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77359813-G-T

http://identifiers.org/hco/2/GRCh38#221436918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77360026-C-A

221436918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360026-C-T

221436931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360039-A-G

221436951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360054-G-T

221436966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360069-T-G

221436974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360077-T-A

221436974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360077-T-C

221436989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360092-C-G

221436989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360092-C-T

221437156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360254-G-A

221437156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360254-G-T

221437191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360289-G-A

221437191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360289-G-T

221437223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360321-G-A

221437223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360321-G-C

221437223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360321-G-T

221437227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360325-G-A

221437227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360325-G-C

221437227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360325-G-T

http://identifiers.org/hco/2/GRCh38#221437276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77360374-C-A

221437276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360374-C-G

221437276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360374-C-T

221437277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360375-T-A

221437277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360375-T-C

221437277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360375-T-G

221437279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360377-G-A

221437279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360377-G-T

221437356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360455-T-A

221437356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77360455-T-C

221437526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77360629-G-A

http://identifiers.org/hco/2/GRCh38#221437545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77360649-C-A

221437545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77360649-C-T

221437589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77360693-G-C

221437589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77360693-G-T

221439723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77361860-T-C

221439836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77361968-G-A

221440365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77362577-G-A

221440365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77362577-G-C

221440365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77362577-G-T

221442426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77364033-C-T

221442451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77364058-C-G

http://identifiers.org/hco/2/GRCh38#221443001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77364606-C-A

221443001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: synonymous variant
orthologous variants: 77364606-C-T

221443033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77364633-A-T

http://identifiers.org/hco/2/GRCh38#221443037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77364637-A-C

221443060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77364660-A-G

221443082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77364672-A-G

221443089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77364679-G-T

221443114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77364704-T-A

221443114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77364704-T-G

221443134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77364724-T-G

221443275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77364861-C-T

221443422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77365047-G-T

221443671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77365287-C-T

221443754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77365377-G-A

221443754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77365377-G-T

221443875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77365519-A-G

221443935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77365578-C-T

221444152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77365806-C-T

221445611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77366161-T-A

221445611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77366161-T-C

221445611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77366161-T-G

http://identifiers.org/hco/2/GRCh38#221445663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77366218-C-A

221445815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77366358-T-A

221445815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77366358-T-C

http://identifiers.org/hco/2/GRCh38#221446038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77366553-C-A

221446038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77366553-C-T

221446105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77366622-T-A

221446105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77366622-T-C

http://identifiers.org/hco/2/GRCh38#221446240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77366775-A-C

221446240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77366775-A-G

221446242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77366777-G-A

221446242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77366777-G-T

221446260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77366796-T-C

http://identifiers.org/hco/2/GRCh38#221446297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77366835-C-A

221446622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77367258-A-G

221446698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77367332-A-G

221446938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77367601-A-G

221447278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77368054-T-C

221447478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, undefined
orthologous variants: 77368203-C-G

221447669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77368420-T-C

221448745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77369512-T-G

221448759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77369526-A-G

221448761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77369528-T-C

221449144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77369994-A-G

221449209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77370059-T-C

221449849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77370667-A-G

221449986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77370806-G-A

221450035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77370875-G-A

221450035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77370875-G-C

221450176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77371010-G-T

221450590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77371165-T-C

221450770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77371274-C-T

221450813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77371320-G-A

221450943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77371451-G-T

221450947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77371455-C-T

221451499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77371805-T-C

221451681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77371991-T-C

221451681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77371991-T-G

221451749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77372211-T-C

221451893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77372575-T-C

221451953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77372636-A-G

221452036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77372717-G-A

221452121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77372799-G-A

221452217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77372971-T-C

221452237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77372991-T-C

221452325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77373074-C-T

221452382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77373092-A-T

http://identifiers.org/hco/2/GRCh38#221452395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77373105-C-A

221452395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77373105-C-T

http://identifiers.org/hco/2/GRCh38#221452507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77373215-C-A

221452507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77373215-C-T

221452541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77373250-C-T

221452601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77373310-G-T

221452880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77373596-C-T

221452966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77373678-T-C

221452966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77373678-T-G

221453430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77374142-C-T

221453456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77374178-T-C

221453728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77374282-T-C

221454394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77374620-G-A

221454650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77374827-G-T

221455514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77375104-G-A

221455514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77375104-G-C

221455514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77375104-G-T

221455526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77375110-G-A

221455526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77375110-G-T

221455701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77375282-T-C

221455736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77375405-A-T

221456042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77375759-T-C

221456057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77375774-A-T

221456154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77375823-G-T

221456521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77376185-T-A

221456521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77376185-T-C

221456582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77376244-G-T

221456683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: synonymous variant
orthologous variants: 77376345-G-A

221456698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: synonymous variant
orthologous variants: 77376360-G-T

221456864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77376633-A-G

221456885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77376662-G-T

221456937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77376724-A-G

221456938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77376725-T-C

221457033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77376866-G-T

221457213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77377176-A-G

221457480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77377563-C-T

221457789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77377793-G-C

221457995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 77377966-T-C

221458021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77377999-T-C

http://identifiers.org/hco/2/GRCh38#221458032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77378010-A-C

221458050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77378024-G-A

221458051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77378025-G-T

http://identifiers.org/hco/2/GRCh38#221458104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77378069-C-A

221458104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77378069-C-T

221458115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77378080-C-T

http://identifiers.org/hco/2/GRCh38#221458128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77378095-C-A

221458128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77378095-C-T

221458138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77378105-G-A

221458138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77378105-G-T

221458232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77378855-C-T

221458398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77379014-C-T

221458599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77379221-G-A

221458810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77379461-C-T

221458830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77379481-T-C

221459019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77379649-C-T

221459095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77379703-T-C

221459172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77379782-G-C

221459220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77379830-C-T

221459503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77380152-G-A

221459668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77380315-T-C

http://identifiers.org/hco/2/GRCh38#221459925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77380583-A-C

221460744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77381393-C-G

221461020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77381648-T-C

221461152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77381774-A-G

221461222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77381844-T-A

221461223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77381845-C-G

221461255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77381876-T-C

221462465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77382607-T-C

221462890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77383657-C-T

221462930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77383697-T-C

221463164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77383928-A-G

221463195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77383956-T-A

221463195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77383956-T-C

221463764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77384515-G-A

221463936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77384695-G-A

221464054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77384805-C-T

221464767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77385576-C-T

221464803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77385617-C-T

221465214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77386541-T-C

221465408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77386708-T-C

221465551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77386861-G-T

221466003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77387313-C-T

221466023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, undefined
orthologous variants: 77387330-T-C

221466233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77387530-C-G

221466337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77387622-T-C

221466366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77387655-A-T

221466425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77387725-C-T

221467185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77388625-A-G

221467196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77388637-G-A

221467260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77388699-C-T

221467430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77388883-T-C

221467491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77388944-T-C

http://identifiers.org/hco/2/GRCh38#221467539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77388994-C-A

221467539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77388994-C-T

221467638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77389072-G-A

221467749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77389129-A-G

221468780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77390009-A-G

http://identifiers.org/hco/2/GRCh38#221469198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77390601-C-A

221469198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77390601-C-T

http://identifiers.org/hco/2/GRCh38#221469360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77390749-A-C

221469360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77390749-A-G

221469405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77390792-G-A

221469537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77390895-T-C

221469537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77390895-T-G

221469590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77390948-T-G

221469867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77391224-T-C

221470135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77391469-C-T

221470162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77391496-C-T

221470195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77391530-G-C

221470201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77391536-T-C

221470254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77391595-C-G

221470885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77392021-C-T

221471033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77392445-G-C

221471033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77392445-G-T

221471088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77392500-T-C

221471522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77392853-T-G

http://identifiers.org/hco/2/GRCh38#221471931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77393193-A-C

221472019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77393293-T-C

221472587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77393831-T-C

221472597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77393841-A-G

221474529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77395726-C-T

221474635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77395849-G-A

221475324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77396353-G-A

221475487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77396538-G-T

221475547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77396596-T-C

221475968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77396931-C-G

221475968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77396931-C-T

221476546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77397334-A-G

221476954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77397739-C-T

221477227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77397995-G-A

221478002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77398583-T-C

221478105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77398711-C-T

221478185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77398792-T-G

221478277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77398876-C-T

221478300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77398899-A-G

http://identifiers.org/hco/2/GRCh38#221478349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77398958-C-A

221478926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77399423-T-C

221478954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77399451-C-G

221479234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77399681-C-T

221479811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77400242-G-A

http://identifiers.org/hco/2/GRCh38#221480202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77400634-C-A

221480369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77400798-A-G

221480370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77400799-G-A

221480427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77400920-T-C

221480525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77401002-A-G

221480528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77401042-C-T

221480550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77401064-C-T

221480565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77401084-G-C

221480680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77401237-C-T

221480775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77401586-C-G

221480775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77401586-C-T

221480917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77401744-A-G

221481156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77401951-T-A

221481214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77402089-G-A

221481214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77402089-G-T

221481419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77402218-A-G

221482383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: synonymous variant
orthologous variants: 77403219-T-G

221482542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77403378-C-G

221482620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77403456-G-A

221482772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77403608-G-T

221484236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77404877-G-A

221484236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77404877-G-T

221484572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77405189-T-G

221484937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77405743-C-T

221485150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77405949-G-A

221485340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77406135-G-A

221485614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77406398-T-C

221485693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77406476-G-T

221486885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77407672-T-C

221486957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77407708-C-G

221486965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77407716-C-T

221486972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77407723-A-G

221487330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77408093-G-C

221487378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77408150-G-A

221489043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77410037-C-G

221489321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77410281-C-T

221490243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77411223-T-A

221490259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77411239-A-G

221490259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77411239-A-T

http://identifiers.org/hco/2/GRCh38#221490410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77411364-C-A

221490737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77411693-G-A

221491136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77412093-T-C

221491292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77412256-A-G

221491335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77412308-A-T

221491714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77412830-C-T

221491887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77412944-G-A

221492382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77413361-T-C

221492587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77413816-A-G

221493233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77414310-T-A

221493233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77414310-T-C

221493346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77414422-A-T

221493352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77414426-A-G

221493369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77414447-T-C

221493421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77414500-G-C

221493517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77414580-C-T

221493569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77414632-G-A

221493860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77414931-T-C

221493946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77415033-C-T

221494176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77415263-G-A

221494479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77415726-G-A

221494614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77415849-G-A

221494831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77416015-G-C

221494855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77416022-G-A

http://identifiers.org/hco/2/GRCh38#221494959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77416102-C-A

221495341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77416448-T-C

http://identifiers.org/hco/2/GRCh38#221495449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77416547-A-C

221495754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77417086-G-A

221496093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77417426-C-T

221496124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77417457-G-T

221496965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77417790-T-A

221496965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77417790-T-C

221497226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77418034-A-T

221497229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77418037-C-T

http://identifiers.org/hco/2/GRCh38#221497239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77418055-C-A

221497239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77418055-C-T

http://identifiers.org/hco/2/GRCh38#221497371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77418167-C-A

221497371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77418167-C-T

221497552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77418306-G-A

http://identifiers.org/hco/2/GRCh38#221498279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77418802-C-A

221498427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77418945-T-C

221500149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77420655-C-T

221500238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77420752-C-T

221500319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77420841-C-T

221500404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77420900-G-A

221500852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77421334-C-T

221500987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77421471-A-T

221501043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77421528-T-C

221501135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77421620-A-G

http://identifiers.org/hco/2/GRCh38#221501224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77421709-A-C

221501224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77421709-A-G

221501285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77421774-T-G

221501291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77421780-T-A

221501291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77421780-T-C

221501312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77421801-T-A

221501414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77422102-T-C

221501414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77422102-T-G

http://identifiers.org/hco/2/GRCh38#221501423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77422111-C-A

221501449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77422137-G-A

221501493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77422182-G-A

221501493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77422182-G-T

221501526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77422205-A-G

http://identifiers.org/hco/2/GRCh38#221502273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77422930-C-A

http://identifiers.org/hco/2/GRCh38#221502404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77423059-C-A

http://identifiers.org/hco/2/GRCh38#221502477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77423120-C-A

221502477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77423120-C-T

221502808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77423454-G-A

221503145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77423788-C-T

221503181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77423826-T-C

221503181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77423826-T-G

221503836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77424647-T-C

221504049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77424861-T-C

221504244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77425061-T-C

221504304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77425111-C-T

221504421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77425332-C-T

221504458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77425402-G-C

221504469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77425413-G-C

221504510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77425450-G-A

221504558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77425587-T-C

221504560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77425589-T-C

221504754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77425759-T-C

221504778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77425782-C-G

221504778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77425782-C-T

221504935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77425912-A-G

221504935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77425912-A-T

http://identifiers.org/hco/2/GRCh38#221504937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77425914-C-A

221505024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77425994-C-T

221505227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77426127-C-T

221505703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77426628-C-T

221505983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77426905-T-C

221505993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77426915-A-G

http://identifiers.org/hco/2/GRCh38#221506036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77426964-A-C

221506270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77427158-A-G

221506281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77427169-A-T

221506310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77427183-T-C

221506341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77427212-T-A

221506405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77427275-G-A

221507381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77428182-T-A

221507404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77428229-C-T

http://identifiers.org/hco/2/GRCh38#221509440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77429954-C-A

221509985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77430943-G-A

http://identifiers.org/hco/2/GRCh38#221510267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77431180-C-A

http://identifiers.org/hco/2/GRCh38#221510718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77431599-A-C

221510718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77431599-A-G

http://identifiers.org/hco/2/GRCh38#221511769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77432338-C-A

221511851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77432441-C-T

221512164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77432744-A-G

221512164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77432744-A-T

221512267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77433057-G-A

221512267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77433057-G-T

221512499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77433382-G-A

221512601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77433470-G-C

221512750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77433586-T-C

221512973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77433814-A-G

221513005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77433855-T-C

http://identifiers.org/hco/2/GRCh38#221513175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77433987-C-A

221513413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77434163-C-T

221513443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77434193-T-A

221513501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77434256-G-A

221513812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77434609-T-C

http://identifiers.org/hco/2/GRCh38#221513822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77434619-A-C

221513992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77434794-C-G

221514140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77434951-G-A

221514140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77434951-G-C

221514303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77435053-G-C

221514413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77435139-A-G

221514424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77435150-A-G

http://identifiers.org/hco/2/GRCh38#221514508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77435234-C-A

221514681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77435399-A-G

221514789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77435493-A-T

221514795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77435499-T-C

221514812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77435518-T-C

221514862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77435573-T-C

221514981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77435740-A-G

221515008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77435764-T-C

221515010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77435766-T-C

http://identifiers.org/hco/2/GRCh38#221515946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77436052-C-A

221515946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77436052-C-T

221515976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77436078-G-A

221516001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77436103-G-A

221517321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77437164-G-A

221517549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77437408-C-T

221517722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77437572-A-T

221518676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77438601-T-C

221518877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77438803-C-T

221519168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77439126-A-G

221519493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77439424-C-T

http://identifiers.org/hco/2/GRCh38#221519697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77439566-A-C

221520002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77439843-C-T

221520404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77440221-T-G

221520420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77440239-T-C

221521113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77440920-T-C

221521303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77441070-T-A

221521303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77441070-T-C

221524077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77442178-G-A

221524317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77442433-A-G

221524456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77442656-G-A

http://identifiers.org/hco/2/GRCh38#221524756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77443017-A-C

221525271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77443532-A-G

221525480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77443770-T-C

221525515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77443803-C-T

221525588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77443868-G-A

221525588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77443868-G-C

221525671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77443945-G-T

221525732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77444011-G-T

221525872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77444142-T-A

221527294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77444752-C-T

http://identifiers.org/hco/2/GRCh38#221527746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77445434-C-A

221528305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77445954-C-T

221528580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77446239-C-T

221528698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77446357-G-A

221528813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77446455-T-C

221529181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77446813-C-T

221529305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77446947-G-A

221529310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77446952-A-G

221529374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77447000-C-T

221529392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77447022-T-C

221529881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77447417-G-C

221530107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77447639-T-G

221530353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77447890-C-T

http://identifiers.org/hco/2/GRCh38#221530623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77448131-C-A

221530985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77448916-T-G

221531000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77448931-A-G

221531101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77449019-C-T

221531359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77449335-C-T

221531389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77449363-T-A

221531390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77449364-G-A

http://identifiers.org/hco/2/GRCh38#221531596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77449551-A-C

221531596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77449551-A-G

221531648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77449600-C-G

221531648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77449600-C-T

221531663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77449606-A-T

221531975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77449808-G-T

221532605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77450023-A-G

http://identifiers.org/hco/2/GRCh38#221532677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77450093-C-A

221532677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77450093-C-T

221532790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77450201-T-C

221532807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77450230-A-G

http://identifiers.org/hco/2/GRCh38#221532810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77450233-C-A

221532810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77450233-C-T

221532828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77450261-C-T

221532829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77450262-T-C

http://identifiers.org/hco/2/GRCh38#221532837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77450271-C-A

221532837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77450271-C-G

221532842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77450276-G-A

http://identifiers.org/hco/2/GRCh38#221532870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77450298-C-A

221532870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77450298-C-T

221532881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77450340-T-C

http://identifiers.org/hco/2/GRCh38#221532897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77450358-C-A

221533031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77450465-G-A

http://identifiers.org/hco/2/GRCh38#221533147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77450564-C-A

221533147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77450564-C-T

221533156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77450574-A-G

221533250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77450646-T-A

221533250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77450646-T-C

221533415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77450847-T-C

221533614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77451045-C-T

221533845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77451257-G-A

221533845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77451257-G-C

221534173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77451520-G-T

221534392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77451698-T-C

221534396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77451703-G-A

221534396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77451703-G-C

221534638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77451922-G-A

http://identifiers.org/hco/2/GRCh38#221535449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77452571-C-A

221535449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77452571-C-G

221535449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77452571-C-T

221535532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77452643-T-G

221535639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77452739-T-C

221535733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77452833-G-A

221535733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77452833-G-T

221537808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77460758-A-G

221538590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77461506-C-T

221538767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77461681-G-A

221539373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77462220-C-T

221539690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77462413-G-A

221539879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77462586-C-T

221539908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77462611-A-G

221539963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77462681-G-A

221540793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77463355-G-A

221540907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77463459-T-C

http://identifiers.org/hco/2/GRCh38#221541202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77463718-A-C

http://identifiers.org/hco/2/GRCh38#221541204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77463720-C-A

221541582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77464014-G-A

221541683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77464123-T-C

221541689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77464129-C-T

221541691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77464131-T-G

221541941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77464350-T-C

221542154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77464550-A-G

221542334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77464721-G-T

221542376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77464763-T-G

221542386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77464773-T-A

221542652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77465027-T-G

http://identifiers.org/hco/2/GRCh38#221543028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77465436-C-A

221543028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77465436-C-T

221543073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77465476-G-A

221543302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77466008-T-A

221543322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77466026-A-G

221543566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77466296-A-G

221549040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77467960-G-A

221549124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77468049-G-A

221549124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77468049-G-T

221549504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77468611-G-A

221549568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77468685-T-C

221549573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77468690-C-T

221551393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77469348-T-C

221551393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77469348-T-G

221551583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77469712-T-A

http://identifiers.org/hco/2/GRCh38#221551754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77469867-C-A

221551754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77469867-C-T

221551767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77469880-G-T

221551843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77469948-T-C

221552015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77470258-C-T

http://identifiers.org/hco/2/GRCh38#221552055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77470287-C-A

221552119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77470351-C-G

221552121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77470356-G-C

221552262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77470488-C-T

221552305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77470530-T-C

221552690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77470914-C-T

221552773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77471024-T-A

221553028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77471430-A-T

221553029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77471431-T-A

221553079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77471493-A-G

221553149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77471564-A-G

221553167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77471580-G-A

221553173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77471586-A-G

221553343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77471755-T-C

221553634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77472035-T-C

221553962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77472367-G-A

221554181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77472584-G-C

221554181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77472584-G-T

221554224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77472627-C-T

221554246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77472649-A-G

http://identifiers.org/hco/2/GRCh38#221554274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77472695-A-C

221554322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77472747-A-G

221554553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77472918-A-T

221554862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77473168-G-A

221554892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77473198-A-G

221555095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77473398-T-C

221555137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77473440-G-C

221555137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77473440-G-T

221555179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77473485-G-T

221555189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77473495-A-T

221555196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77473502-T-C

221555196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77473502-T-G

http://identifiers.org/hco/2/GRCh38#221555249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77473555-C-A

221555261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77473572-A-G

221555269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77473580-T-C

221555283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77473594-T-C

221555342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77473654-G-C

http://identifiers.org/hco/2/GRCh38#221556042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77474368-C-A

221557941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77477560-A-G

221558411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77477877-A-G

221558733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77478215-G-C

221559100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77478599-A-G

221559100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77478599-A-T

221559215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77478801-A-T

221559782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77479225-C-G

221559909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77479299-T-G

221559972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77479381-C-T

221560353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77479761-C-G

221560353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77479761-C-T

http://identifiers.org/hco/2/GRCh38#221560368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77479776-C-A

http://identifiers.org/hco/2/GRCh38#221560720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77480115-A-C

221560970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77480420-C-G

221560970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77480420-C-T

221561103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77480577-G-A

221561103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77480577-G-C

221561111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77480585-G-A

221561111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77480585-G-C

http://identifiers.org/hco/2/GRCh38#221561124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77480598-C-A

221561124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77480598-C-T

221561544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77481027-T-G

221561581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77481064-T-C

221561767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77481262-T-C

221562296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77481861-T-G

221562389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77481938-C-T

221562581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77482118-C-T

221562766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77482271-C-G

http://identifiers.org/hco/2/GRCh38#221562908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77482390-C-A

221563403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77482859-C-T

221563432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77482888-C-T

221563575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77483031-G-A

221563724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 77483178-C-T

http://identifiers.org/hco/2/GRCh38#221564191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77483645-C-A

221564191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77483645-C-G

221564191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77483645-C-T

221564383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77483837-C-T

221564505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77483953-G-A

221564505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77483953-G-T

http://identifiers.org/hco/2/GRCh38#221564518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77483966-C-A

221564518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77483966-C-T

http://identifiers.org/hco/2/GRCh38#221564519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77483967-A-C

221564526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77483974-A-G

221564877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77484373-T-A

221565112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77484590-C-T

221565186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77484706-G-A

221565220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77484745-T-C

221565321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77484860-T-A

221565344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77484887-C-G

221565486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77485042-G-A

221565494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77485050-A-T

221565721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77485250-G-A

221566172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77485656-A-G

http://identifiers.org/hco/2/GRCh38#221566374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77485848-A-C

221567121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77486713-A-G

http://identifiers.org/hco/2/GRCh38#221567251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77486853-A-C

221567548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487175-T-C

221567608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487236-G-A

221567949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487574-G-T

221567953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487578-T-C

221568010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487641-C-T

221568101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487730-C-T

221568240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487840-T-A

221568373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487978-G-A

http://identifiers.org/hco/2/GRCh38#221568395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77488000-A-C

http://identifiers.org/hco/2/GRCh38#221568605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77488210-C-A

221568605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77488210-C-G

221568605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77488210-C-T

http://identifiers.org/hco/2/GRCh38#221568620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77488225-C-A

221568620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77488225-C-T

221568884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77488501-G-A

http://identifiers.org/hco/2/GRCh38#221568907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77488523-C-A

221568963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77488578-T-C

http://identifiers.org/hco/2/GRCh38#221569290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77488913-C-A

221569311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77488934-T-C

221569402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77489023-T-C

221569561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77489186-A-G

221569562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77489187-G-A

221569686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77489304-G-A

http://identifiers.org/hco/2/GRCh38#221569777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77489396-C-A

221569777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77489396-C-T

221570222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77489794-T-G

221570274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77489853-G-C

http://identifiers.org/hco/2/GRCh38#221570326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77489921-C-A

221570326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77489921-C-G

221570356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77489965-G-A

221570356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77489965-G-T

http://identifiers.org/hco/2/GRCh38#221570431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77490059-C-A

221570558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77490176-A-G

221570560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77490178-G-A

http://identifiers.org/hco/2/GRCh38#221570575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77490193-A-C

221570880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77490401-C-T

221572021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77491427-A-G

http://identifiers.org/hco/2/GRCh38#221572055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77491461-C-A

http://identifiers.org/hco/2/GRCh38#221572107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77491525-C-A

221572107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77491525-C-G

221572107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77491525-C-T

221572145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77491565-G-A

221572145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77491565-G-T

221572366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77491786-G-A

221572366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77491786-G-T

221572378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77491798-G-A

221572378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77491798-G-C

221572451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77491872-T-A

221572451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77491872-T-C

221572451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77491872-T-G

http://identifiers.org/hco/2/GRCh38#221572463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77491884-C-A

221572463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron variant
orthologous variants: 77491884-C-T

http://identifiers.org/hco/2/GRCh38#221572525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77491945-C-A

221572525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77491945-C-G

221572525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77491945-C-T

http://identifiers.org/hco/2/GRCh38#221572554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77491958-C-A

221572556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77491960-C-T

221572622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492033-A-G

221572622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492033-A-T

http://identifiers.org/hco/2/GRCh38#221572629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77492040-C-A

221572629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492040-C-G

221572629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492040-C-T

221572647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492058-A-G

221572726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492139-C-T

221572757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492177-G-A

221572853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492271-G-T

221572889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492309-C-T

http://identifiers.org/hco/2/GRCh38#221572935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77492346-C-A

221572935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492346-C-G

http://identifiers.org/hco/2/GRCh38#221572969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77492370-C-A

221572969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492370-C-T

http://identifiers.org/hco/2/GRCh38#221573024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77492411-C-A

221573024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492411-C-T

221573069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492457-A-G

221573081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492479-G-T

221573095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492495-G-T

221573276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492657-G-A

221573276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492657-G-C

http://identifiers.org/hco/2/GRCh38#221573288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77492681-C-A

221573288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492681-C-T

221573323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492709-G-A

221573323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492709-G-T

221573384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492796-G-A

221573384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492796-G-T

221573453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77492850-G-A

221573614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77493007-G-A

221573635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 77493026-G-A

221573635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 77493026-G-T

http://identifiers.org/hco/2/GRCh38#221573675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77493063-C-A

221573675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77493063-C-T

221573780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 77493157-A-G

221573799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77493173-G-A

221573799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77493173-G-C

221573799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77493173-G-T

http://identifiers.org/hco/2/GRCh38#221573900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#77493245-C-A

221573919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77493264-G-A

221573919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77493264-G-T

221573963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 77493302-T-C

http://identifiers.org/hco/2/GRCh38#221573988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77493327-C-A

221573988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77493327-C-T

http://identifiers.org/hco/2/GRCh38#221574109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3388
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#77493454-C-A