http://identifiers.org/hco/7/GRCh38#30771456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#55180459-C-A

30771456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55180459-C-G

30771456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55180459-C-T

http://identifiers.org/hco/7/GRCh38#30771466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#55180470-C-A

30771466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55180470-C-T

http://identifiers.org/hco/7/GRCh38#30771480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#55180484-C-A

30771480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55180484-C-T

30771520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 55180518-G-A

30771610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55180608-A-G

30771610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55180608-A-T

30771646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55180646-A-G

http://identifiers.org/hco/7/GRCh38#30771658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#55180658-C-A

30771658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55180658-C-G

30771658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55180658-C-T

30771661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55180661-T-A

30771661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55180661-T-C

30771661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55180661-T-G

http://identifiers.org/hco/7/GRCh38#30771674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#55180674-C-A

30771674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55180674-C-T

30771861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55180856-G-C

30772216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55181106-A-G

30772361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55181314-G-A

30772403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55181355-A-G

30772805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55182030-T-C

30772895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55182100-A-G

30773843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55183625-C-G

30774201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55183955-C-T

30774273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55184032-C-T

30774288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55184041-C-T

30774310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55184063-T-G

http://identifiers.org/hco/7/GRCh38#30774463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55184167-C-A

http://identifiers.org/hco/7/GRCh38#30774564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55184248-C-A

30774668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55184312-C-T

30774742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55184379-C-T

30774812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55184439-C-T

30774815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55184442-G-C

30774815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55184442-G-T

30774994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55184609-A-G

30774998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55184613-T-C

30775084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55184692-A-G

http://identifiers.org/hco/7/GRCh38#30775091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55184699-C-A

30777699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187551-G-A

30777770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187608-A-G

30777935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187729-C-G

http://identifiers.org/hco/7/GRCh38#30777941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55187735-A-C

30777967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187742-T-A

30778026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187793-G-A

30778132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187894-T-C

30778217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55187992-T-C

30778281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188063-G-T

30778372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188172-T-A

30778372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188172-T-G

30778446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55188249-A-G

http://identifiers.org/hco/7/GRCh38#30778589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55188373-C-A

30778589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188373-C-T

30778596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188380-T-G

30778758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188489-C-T

30778759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188490-G-A

30778768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188499-G-T

30778834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188560-C-G

30778896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188619-C-T

30778899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188699-G-T

30778982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188760-T-A

30779074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188847-G-A

30779158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188913-T-C

30779232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188979-T-A

http://identifiers.org/hco/7/GRCh38#30779238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55188985-C-A

30779282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189027-C-T

30779853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55189860-A-G

30779906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55189910-C-T

30779907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55189911-A-G

30779981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55189979-T-C

30780017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55190010-G-T

30780036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55190030-G-T

http://identifiers.org/hco/7/GRCh38#30780290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55190234-C-A

30780532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55190469-G-A

30780872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55191480-C-T

30781009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55191624-G-T

30781070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55191664-G-A

30781070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55191664-G-T

30781095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55191687-T-C

30781193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55191797-A-G

30781365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55191985-G-T

http://identifiers.org/hco/7/GRCh38#30781461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55192061-C-A

http://identifiers.org/hco/7/GRCh38#30781696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55193263-C-A

30781758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55193291-G-A

30781860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55193376-T-A

http://identifiers.org/hco/7/GRCh38#30781919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55193432-C-A

30781919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55193432-C-T

30781937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55193451-G-A

30781937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55193451-G-T

30782009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55193524-A-G

30782021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55193536-A-G

30782047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55193562-C-G

30782047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55193562-C-T

30782139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55193654-C-T

30782157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55193672-C-G

30782157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55193672-C-T

30785592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55195092-G-C

30785597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55195097-T-A

30785597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55195097-T-C

30785745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55195203-A-G

30785790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55195248-C-T

30785825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 55195283-C-T

30785863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55195321-A-G

30785878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55195336-C-T

30785883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55195341-T-G

30785901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55195362-T-C

30785901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55195362-T-G

30785977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55195438-C-T

http://identifiers.org/hco/7/GRCh38#30786106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55195536-C-A

30786106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55195536-C-G

30786114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55195544-G-C

30786114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55195544-G-T

30786124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55195554-G-A

30786124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55195554-G-T

30786131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55195557-G-T

http://identifiers.org/hco/7/GRCh38#30786132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55195558-C-A

30786132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55195558-C-T

30786217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55195634-T-A

30786217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55195634-T-C

30786221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55195638-T-A

30786221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55195638-T-C

30786225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55195642-G-T

30786236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55195653-G-T

http://identifiers.org/hco/7/GRCh38#30786247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55195664-C-A

http://identifiers.org/hco/7/GRCh38#30786310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55195731-C-A

http://identifiers.org/hco/7/GRCh38#30786311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55195732-A-C

30786311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55195732-A-T

http://identifiers.org/hco/7/GRCh38#30786725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55195801-C-A

30786734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55195810-T-G

30786811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55195887-A-G

30787019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55196066-T-C

http://identifiers.org/hco/7/GRCh38#30787269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55196142-C-A

30787282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55196155-T-C

30787632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55196597-C-T

30787650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55196614-A-G

30787668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55196628-T-A

30787755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55196705-G-A

30787860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55196807-T-G

30788287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55197631-G-A

30788427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55197761-T-C

30788538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55197882-A-G

30788792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55198318-C-T

30788793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55198319-G-A

30789156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55198849-A-G

30789168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55198861-G-A

30789192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55198882-G-T

30789203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55198895-G-A

30789203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55198895-G-T

30789624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199214-G-C

30789705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199293-C-T

30789715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199303-T-C

30789717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199305-C-T

30789733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199319-G-A

30789733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199319-G-T

30789779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199365-C-G

30790183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199732-A-G

30790205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199752-G-A

30790205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199752-G-C

30790378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199892-A-G

30790383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199897-G-A

30791107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55200924-C-T

30791159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55200977-C-T

30791182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55201000-C-G

30791405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55201220-G-C

30791405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55201220-G-T

30791563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55201342-C-T

http://identifiers.org/hco/7/GRCh38#30791601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55201378-C-A

http://identifiers.org/hco/7/GRCh38#30791627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55201404-A-C

http://identifiers.org/hco/7/GRCh38#30791689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55201466-C-A

http://identifiers.org/hco/7/GRCh38#30791697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55201474-C-A

30791697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55201474-C-T

30792045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55201645-G-A

30792173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55201751-G-A

30792191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55201770-T-C

30792233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55201811-A-T

30792546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55202058-A-G

30792639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55202141-G-A

30792802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55202347-T-C

http://identifiers.org/hco/7/GRCh38#30792812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55202357-A-C

30792892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55202431-A-G

30795540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55208948-C-T

http://identifiers.org/hco/7/GRCh38#30795771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55209164-C-A

30795795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55209188-C-T

30795858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55209236-T-C

30795951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55209323-T-C

30796008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55209372-T-C

30796095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55209441-G-A

30796124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55209465-T-A

30796168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55209511-C-T

30796246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55209580-G-A

30800899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55209940-A-G

30801094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210109-G-T

30801368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210391-G-A

30801368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210391-G-C

30801406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210421-C-G

30801445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210455-C-T

30801449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210459-C-G

30801510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210475-C-T

30801548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210510-T-C

30801680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210626-A-G

30801681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210627-T-C

30801683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210629-G-A

30801751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210673-A-G

30801793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210715-T-C

30802004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210858-A-G

30802160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55211005-G-T

30802227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55211093-A-G

30802376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55211232-C-T

30802430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55211285-G-A

30802447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55211301-C-T

30802535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55211389-A-G

http://identifiers.org/hco/7/GRCh38#30802559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55211413-A-C

30802770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55211579-A-G

http://identifiers.org/hco/7/GRCh38#30802932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55211673-C-A

30802932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55211673-C-T

http://identifiers.org/hco/7/GRCh38#30803042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55211731-C-A

http://identifiers.org/hco/7/GRCh38#30803045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55211734-C-A

30803045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55211734-C-T

http://identifiers.org/hco/7/GRCh38#30803076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55211740-C-A

30803076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55211740-C-G

30803252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55211889-T-C

30803482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212056-G-T

30803491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212065-T-C

30803542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212106-A-G

30803542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212106-A-T

30804170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55212630-C-T

30804387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212847-C-T

30804499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55212960-C-T

http://identifiers.org/hco/7/GRCh38#30805019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55213823-C-A

30805019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55213823-C-T

30805193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55214196-C-T

30805409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55214370-C-T

30805410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55214371-G-A

30805517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55214534-G-A

30805621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55214644-G-A

30805734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55214771-T-G

30805876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55214917-G-A

30806103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55215164-C-T

30806733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55216223-T-C

30806788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55216280-G-A

30806853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55216320-G-C

30807104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55216539-G-C

30807330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55216700-C-T

30807386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55216758-C-T

30807394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55216766-A-G

30812242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217135-A-G

30812276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217184-G-A

30812276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217184-G-C

30812276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217184-G-T

30812298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217214-T-A

30812583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217480-C-T

30812969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217851-T-A

30812978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217860-C-T

30813092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217963-T-C

http://identifiers.org/hco/7/GRCh38#30813199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55218059-A-C

http://identifiers.org/hco/7/GRCh38#30813220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55218230-C-A

30813220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218230-C-T

30813232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218282-A-T

30813273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218345-A-G

30813735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218793-C-G

30813739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218797-G-A

30813789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218846-C-T

30813808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218863-A-G

30814270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55220264-G-T

30814276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55220270-C-T

30814385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55220358-T-G

30814426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55220393-C-G

30814426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55220393-C-T

30814453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55220420-G-A

30814498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55220476-C-T

30814998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55220895-C-T

30815405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55221351-C-G

30815448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55221398-T-G

30815667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55221596-A-G

30816129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55222470-T-A

30816164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55222504-G-C

30816170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55222510-C-T

http://identifiers.org/hco/7/GRCh38#30816451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55222781-A-C

30816642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55222948-G-T

30816902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223442-A-G

30816979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223522-G-T

http://identifiers.org/hco/7/GRCh38#30817092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55223638-A-C

30817149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223704-A-G

http://identifiers.org/hco/7/GRCh38#30817346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55223884-C-A

30817352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223890-G-A

30817701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224117-C-T

30818012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224280-A-G

30818012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224280-A-T

30818144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224381-A-G

30818304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224536-G-A

30818435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224685-A-G

30818706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55225018-C-T

30819191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55225662-G-A

30819194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55225665-C-G

30819194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55225665-C-T

http://identifiers.org/hco/7/GRCh38#30819437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55225911-C-A

30819437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55225911-C-T

30819552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226017-C-G

30819552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226017-C-T

30819571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226034-A-T

30819596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226059-C-T

30819647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226107-T-C

30819812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226252-G-A

30819815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226257-A-G

30819840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226280-A-G

30820415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226733-G-A

30820552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226844-T-C

http://identifiers.org/hco/7/GRCh38#30820769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55227050-C-A

30820769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55227050-C-G

30820775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55227056-G-C

30821016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55227265-G-A

30821219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55227451-G-A

30821571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55227802-C-T

30821677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55227877-C-T

30822041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55228157-T-C

30822120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55228207-G-A

30822120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55228207-G-T

30824900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55229554-C-G

30824904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55229558-G-A

30824917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55229571-C-T

30824921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55229575-G-A

30824971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55229618-A-G

30825151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55229765-T-G

30825520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230093-G-A

30825591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230163-C-T

30825592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230164-A-G

30826149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230603-T-C

30826411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230790-G-A

30826464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230834-A-G

30826874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55231201-G-A

30826893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55231222-C-T

30827058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55231371-G-A

30827061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55231374-G-A

30827092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55231408-C-G

30827092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55231408-C-T

30827100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55231416-G-C

30827375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55231626-C-T

30827443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55231701-T-G

30827535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55231751-G-T

30827572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55231783-G-T

30827753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55231912-G-A

30828077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55232193-T-C

30828103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55232219-G-T

http://identifiers.org/hco/7/GRCh38#30828268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55232328-A-C

30828453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55232448-C-T

30828547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55232492-G-A

30828547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55232492-G-T

30828571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55232514-A-T

http://identifiers.org/hco/7/GRCh38#30828745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55232659-C-A

30828766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55232680-G-A

http://identifiers.org/hco/7/GRCh38#30828769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55232693-C-A

30828769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55232693-C-T

30828770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55232694-A-G

30828770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55232694-A-T

30828812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55232807-G-A

30828812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55232807-G-T

30828834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55232832-T-A

30828834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55232832-T-C

30828834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55232832-T-G

30828964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55233182-C-G

30828965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55233183-T-C

30829071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55233237-T-C

30829158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55233326-T-A

http://identifiers.org/hco/7/GRCh38#30829721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55233865-A-C

30829776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55233923-T-G

30830027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55234144-C-T

30830077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55234165-G-A

30830078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55234166-G-A

30831982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55235536-G-A

http://identifiers.org/hco/7/GRCh38#30832063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55235617-C-A

http://identifiers.org/hco/7/GRCh38#30832065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55235619-C-A

30832065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55235619-C-G

30832384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55235898-C-T

30832427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55235941-C-T

30832449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55235948-A-G

30835884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55236744-G-A

30836313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237281-C-G

http://identifiers.org/hco/7/GRCh38#30836369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55237317-C-A

30836369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237317-C-T

30836452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237350-G-A

30836452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237350-G-T

30836516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237405-T-C

30836519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237409-G-T

30836624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237498-A-T

30836639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237502-G-A

30836640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237503-G-A

30836675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55237537-T-A

30836710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55237572-A-G

30836710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55237572-A-T

http://identifiers.org/hco/7/GRCh38#30836782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55237648-C-A

30836782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237648-C-T

30836794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237660-G-A

30836872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237751-A-G

30837033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237915-C-T

30837036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237918-C-T

30837087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237963-C-T

30837316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55238181-C-T

30837532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55238380-C-T

30837565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55238396-C-G

30837671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55238503-G-A

30837725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55238556-G-A

30837767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55238597-C-T

30837842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55238648-G-C

http://identifiers.org/hco/7/GRCh38#30837881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55238692-A-C

30837881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55238692-A-G

30838557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55238939-C-T

30838679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55239059-G-A

30838695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55239076-C-T

30838822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55239364-A-G

30838877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55239418-A-T

30838999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55239523-A-G

30839220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55239724-T-G

30839327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55239831-C-T

30839342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55239846-G-C

30839342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55239846-G-T

30839353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55239857-T-C

http://identifiers.org/hco/7/GRCh38#30839406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55239907-A-C

http://identifiers.org/hco/7/GRCh38#30839408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55239909-C-A

30839408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55239909-C-T

http://identifiers.org/hco/7/GRCh38#30839419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55239917-C-A

30839588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55240038-C-T

30839742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55240169-G-A

30839769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55240188-A-G

30839835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55240251-C-T

30839855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55240267-C-G

30839855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55240267-C-T

http://identifiers.org/hco/7/GRCh38#30840544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55240609-C-A

30840544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55240609-C-T

30840647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55240666-A-G

30840678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55240686-G-A

30840858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55240859-T-G

http://identifiers.org/hco/7/GRCh38#30840949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55240938-C-A

30840949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55240938-C-G

30841000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55240989-G-T

30841050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55241037-C-T

30842601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55241581-G-T

30842893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55241837-G-T

30843077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55241972-C-T

30843135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55242034-G-A

30843273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55242176-G-A

30843409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55242287-C-G

30843515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55242379-C-T

30843651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55242467-G-A

30843698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55242513-G-C

30844560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55244004-G-A

30844577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55244018-G-C

30844708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55244133-G-A

30845041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55244424-G-T

30845074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55244458-C-T

30845103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55244475-G-C

30845150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55244520-A-G

30845176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55244540-A-G

30845189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55244553-C-T

30845883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55250111-C-G

30845883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55250111-C-T

30845936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55250165-G-A

30846049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55250255-G-A

30846098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55250295-G-A

30846152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55250347-T-G

30846274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55250467-A-G

30846274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55250467-A-T

30846412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55250579-T-G

30846423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55250589-C-T

30846536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55250708-A-G

30846640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55250828-G-A

30847125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55250905-G-C

http://identifiers.org/hco/7/GRCh38#30847258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55251044-A-C

30847585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55251329-G-A

30847585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55251329-G-T

30848201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55251775-G-A

30848443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55251988-A-G

30848582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55252091-G-C

30848888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55252397-G-T

30848945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55252435-C-T

http://identifiers.org/hco/7/GRCh38#30848947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55252437-C-A

30848947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55252437-C-T

30848961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55252446-G-T

30849054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55252545-G-A

30849365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55252879-T-C

30849366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55252880-A-T

30849426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55252941-C-T

30849451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55252966-T-G

30849631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55253166-T-A

30849642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55253175-T-G

http://identifiers.org/hco/7/GRCh38#30850448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55253536-C-A

30850486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55253571-G-A

30850486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55253571-G-C

30850486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55253571-G-T

30850517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55253602-G-A

http://identifiers.org/hco/7/GRCh38#30850695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55253717-C-A

30850695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55253717-C-T

30850753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55253743-C-T

30850886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55253853-T-G

30851116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254046-G-T

30851203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254100-T-C

30851210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254105-C-T

30851212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254107-A-G

30851343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254249-C-T

30851472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254381-G-C

30851532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254424-T-A

http://identifiers.org/hco/7/GRCh38#30851735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55254588-C-A

30851907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254775-C-G

30852084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254901-T-C

30852157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254973-G-C

30852161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254977-G-C

30852231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55255047-G-A

30852434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55255272-G-A

30852434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55255272-G-T

30852593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55255441-G-A

30852650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55255478-G-A

30852727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55255552-C-T

30853021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55255787-C-T

30853043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55255815-C-G

30853062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55255833-T-C

30853198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55255941-C-T

30853199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55255942-G-A

30853353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55256034-G-A

30853353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55256034-G-C

30853380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55256056-T-C

30853420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55256096-T-C

http://identifiers.org/hco/7/GRCh38#30853451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55256127-A-C

30853451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55256127-A-G

30853451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55256127-A-T

30853519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55256192-G-A

30853519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55256192-G-T

http://identifiers.org/hco/7/GRCh38#30853554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55256224-C-A

30853554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55256224-C-T

30853581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55256253-T-C

30853704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55256361-C-T

30853810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55256439-C-T

http://identifiers.org/hco/7/GRCh38#30854081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55256709-A-C

30854176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55256777-A-G

30854235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55256821-C-T

30854886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55257220-C-T

30855062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55257376-A-G

30855131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55257451-G-A

30855131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55257451-G-C

30855359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55257624-C-T

30855542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55257742-G-T

30855603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55257789-G-T

30855818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55257994-T-C

30855844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55258025-C-G

30856008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55258185-C-T

30856224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55258365-A-G

30856263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55258389-C-T

30856622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55258727-G-T

30856663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55258741-G-A

30856685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55258759-A-G

30856815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55258805-G-A

30857199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55259151-T-C

30857293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55259200-A-G

30857293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55259200-A-T

30857337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55259245-G-A

30857455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55259346-C-T

30857478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55259385-T-C

30857558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55259449-C-T

30857655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55259510-G-T

30857660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55259515-G-A

30857660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55259515-G-T

30857785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55259527-A-G

http://identifiers.org/hco/7/GRCh38#30857790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55259532-C-A

30857858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55259602-A-G

30857936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55259675-G-T

30858476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55261061-G-A

30858476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55261061-G-C

30858476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55261061-G-T

http://identifiers.org/hco/7/GRCh38#30858493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55261075-C-A

30858701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55261213-T-C

30858787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55261301-G-A

http://identifiers.org/hco/7/GRCh38#30858817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55261333-C-A

30858830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55261346-G-A

30858830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55261346-G-T

30858883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55261367-G-T

30859016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55261480-A-G

30859103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55261556-G-T

http://identifiers.org/hco/7/GRCh38#30859120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55261600-C-A

30859120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55261600-C-G

30859152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55261633-G-T

http://identifiers.org/hco/7/GRCh38#30859161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55261648-C-A

30859284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55261758-C-T

30859354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55261822-G-A

30859362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55261830-T-C

30860067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55262184-G-A

30860269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55262349-C-T

30860318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55262395-T-G

http://identifiers.org/hco/7/GRCh38#30860556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55262631-C-A

30860556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55262631-C-T

30860713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55262797-T-C

30860783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55262865-T-C

30860969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55263015-A-G

30861002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55263034-G-A

30861002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55263034-G-C

http://identifiers.org/hco/7/GRCh38#30861365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55263372-C-A

30861616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55263542-G-A

30861682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55263615-C-T

30861694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55263671-A-T

30861790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55263758-T-C

30862015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55263930-G-C

30862193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264058-G-C

30862392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264186-C-T

30862603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264267-C-T

30862624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264288-A-G

30862769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264410-G-A

30862769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264410-G-T

30862789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264423-C-T

30862856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264476-T-A

30863090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264659-G-C

30863187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264752-A-G

30863353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264903-G-C

30863355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264905-G-A

30863361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264911-G-T

30863434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264985-G-T

30863495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55265037-T-C

30863503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55265045-G-A

30863746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55265204-G-A

30863747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55265205-G-A

30864243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55265639-C-T

30864256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55265649-T-C

30864480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55265853-A-G

30864645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55266012-G-A

30864645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55266012-G-T

30864672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55266022-A-G

30864732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55266079-C-G

30864884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55266223-T-C

30864975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55266298-C-T

30865037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55266353-A-G

30865151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55266459-T-C

30865702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55267505-T-G

30865800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55267592-T-C

30865857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55267647-C-T

30866076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55267845-G-C

30866265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55268032-C-T

30866338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55268113-G-T

30866590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55268367-C-T

http://identifiers.org/hco/7/GRCh38#30866747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55268539-A-C

30867191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55268914-C-T

30867231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55268943-G-C

30867356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269069-T-G

30867422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269120-C-T

30867706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269354-G-A

30867900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269482-A-G

30868424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269966-G-A

30868424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269966-G-C

30868510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55270046-T-G

30868602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55270110-G-A

30868751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55270223-T-C

30869024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55270415-C-T

30869859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55271498-A-G

30870208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55271839-C-G

30870208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55271839-C-T

30870399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55272027-C-T

30870488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55272114-C-T

30870610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55272227-C-G

30870673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55272342-A-G

30870793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55272438-G-A

30871189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55272582-C-T

30871300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55272675-C-G

30871378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55272752-C-T

30871452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55272818-C-T

30871572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55272913-G-A

30871597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55272939-C-T

30871635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55272975-A-T

30871748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55273126-G-A

30871748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55273126-G-C

30872150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274596-G-T

30872153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274599-T-C

30872170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274615-G-A

30872170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274615-G-C

30872170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274615-G-T

30872211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274638-G-C

30872326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274756-C-T

http://identifiers.org/hco/7/GRCh38#30872349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55274777-C-A

30872349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274777-C-G

30872349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274777-C-T

http://identifiers.org/hco/7/GRCh38#30872379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55274794-C-A

30872379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274794-C-T

http://identifiers.org/hco/7/GRCh38#30872382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55274797-C-A

30872382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274797-C-G

30872382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274797-C-T

http://identifiers.org/hco/7/GRCh38#30872453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55274834-C-A

30872453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274834-C-T

30872578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274946-T-C

30872603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274975-G-T

30872646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55275013-C-T

30873038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55275302-G-A

30873043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55275307-A-G

30873088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55275351-G-A

30873212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55275469-G-A

30873214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55275471-G-A

30873265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55275521-C-T

30873295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55275555-G-A

30873535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55275786-T-G

30873543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55275797-G-A

30873808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55276191-T-A

30873816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55276375-G-T

30874122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55276659-C-T

http://identifiers.org/hco/7/GRCh38#30874171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55276703-C-A

30874171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55276703-C-T

30874230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55276749-G-A

30874230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55276749-G-C

30874423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55276936-A-T

http://identifiers.org/hco/7/GRCh38#30874474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55276970-A-C

30874652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55277136-C-T

30874886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55277308-G-A

30874886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55277308-G-C

30875334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55277758-A-G

http://identifiers.org/hco/7/GRCh38#30875380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55277808-C-A

http://identifiers.org/hco/7/GRCh38#30875403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55277831-C-A

30875403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55277831-C-G

30875403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55277831-C-T

30875437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55277866-C-T

30875454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55277886-A-T

30875467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55277902-G-A

30875527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55277960-T-A

30875583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55278016-C-T

http://identifiers.org/hco/7/GRCh38#30875590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55278023-C-A

30875590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55278023-C-T

30875690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278117-G-T

30875757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278191-T-C

http://identifiers.org/hco/7/GRCh38#30875768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55278202-C-A

30875768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278202-C-T

30875796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278229-G-A

30875796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278229-G-T

30875844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278273-C-T

30875899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278325-G-T

30875981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278422-G-T

30876261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278622-A-T

30876634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278951-T-G

30876658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278969-A-G

30876761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55279062-T-G

http://identifiers.org/hco/7/GRCh38#30877024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55279283-C-A

30877299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55279526-G-T

30877385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55279607-T-C

30877498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55279709-C-T

30877654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55279862-C-G

30877654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55279862-C-T

30877655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55279863-C-G

30877655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55279863-C-T

30877673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55279881-T-G

30880490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55283096-G-A

30880663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55283201-G-A

30880787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55283302-G-A

30881037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55283537-C-T

http://identifiers.org/hco/7/GRCh38#30881158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55283647-C-A

30881158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55283647-C-G

30881613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55284634-C-G

30881649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55284687-G-T

30881714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55284755-G-A

30881954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55284988-T-C

30882095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55285087-T-C

30882300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55285259-C-G

http://identifiers.org/hco/7/GRCh38#30882402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55285346-A-C

http://identifiers.org/hco/7/GRCh38#30882434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55285376-C-A

30882434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55285376-C-T

30882436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55285378-T-C

30882436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55285378-T-G

30882501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55285411-A-G

30882624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55285527-C-T

30882626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55285529-G-T

30882752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286075-G-A

30882785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286109-T-C

30882785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286109-T-G

30882825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286149-A-G

30882825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286149-A-T

http://identifiers.org/hco/7/GRCh38#30882864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55286190-C-A

30882864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286190-C-G

30882928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55286254-C-G

30882935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55286261-A-G

30883016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286341-T-G

30883078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286407-G-T

30883113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286441-G-C

30883113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286441-G-T

30883356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286545-G-A

http://identifiers.org/hco/7/GRCh38#30883395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55286580-A-C

30883395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286580-A-G

30883407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286592-G-A

30883407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286592-G-T

30883429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286618-A-G

30883654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286834-T-C

30883690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286856-G-A

30883690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286856-G-T

30883718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286888-A-G

30883772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55286949-G-A

30884124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55287233-G-C

30884166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55287277-G-A

30884751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55287809-C-T

30884800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55287860-C-T

30884875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55287964-G-A

30884875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55287964-G-C

30885216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55288354-G-A

30885254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55288392-C-T

30886169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289416-G-A

30886202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289450-G-A

http://identifiers.org/hco/7/GRCh38#30886301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55289536-A-C

30886317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289552-C-T

30886340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289573-A-G

30886405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289635-C-T

30886417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289647-C-G

30886450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289700-T-G

30886621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289856-G-A

30886630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289865-C-G

30886923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55290147-A-G

30886971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55290197-C-T

30887013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55290239-C-T

30887014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55290240-G-A

http://identifiers.org/hco/7/GRCh38#30887141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55290345-C-A

30887141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55290345-C-G

30887141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55290345-C-T

30887541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55290634-G-A

30887541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55290634-G-T

30887599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55290700-C-T

30887671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55290765-G-A

30887687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55290766-C-T

30887763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55290824-G-T

30887852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55290901-G-A

30887944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55290993-G-A

http://identifiers.org/hco/7/GRCh38#30887990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55291038-C-A

30888158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55291199-G-T

30888203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55291242-G-A

30888367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55291399-T-C

30888497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55291495-G-A

30888696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55291657-C-G

30888754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55291708-T-C

30888915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55291850-G-A

30888989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55291911-A-T

30889234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55292173-T-C

30889278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55292215-G-A

30889441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55292358-T-G

30889502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55292411-G-A

30889620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55292529-G-T

30889679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55292595-A-T

30889822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55292706-A-G

30889876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55292761-T-C

http://identifiers.org/hco/7/GRCh38#30890032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55292853-A-C

30890043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55292864-G-T

30890113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55292946-G-A

30890113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55292946-G-T

30890168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55292992-G-A

30890202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55293020-T-C

30890688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55293485-G-A

30890933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55294366-A-G

30891302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55294688-G-A

30891302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55294688-G-C

http://identifiers.org/hco/7/GRCh38#30891395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55294754-C-A

30891395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55294754-C-T

30891514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55294860-A-G

30891514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55294860-A-T

30891527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55294874-C-G

30891813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55295161-G-A

30891813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55295161-G-T

30891825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55295172-T-A

30891826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55295173-G-A

30891826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55295173-G-T

30891833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55295180-A-T

http://identifiers.org/hco/7/GRCh38#30891855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55295195-C-A

30891855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55295195-C-T

30892315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55295579-G-A

30892315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21916
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55295579-G-T