http://identifiers.org/hco/17/GRCh38#47323410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104576234-C-A

47323538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104576343-G-A

47323538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104576343-G-T

http://identifiers.org/hco/17/GRCh38#47323570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#104576376-C-A

47323570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 104576376-C-T

47323837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 104576595-T-A

47323843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 104576600-T-C

47323843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 104576600-T-G

47323883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104576626-G-A

47323883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104576626-G-C

47323883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104576626-G-T

47323901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104576643-T-C

47323901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104576643-T-G

47323941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, undefined
orthologous variants: 104576682-G-A

47323941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, undefined
orthologous variants: 104576682-G-T

http://identifiers.org/hco/17/GRCh38#47323959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#104576700-C-A

47323959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104576700-C-T

http://identifiers.org/hco/17/GRCh38#47323968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104576709-C-A

47323968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104576709-C-T

47323969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104576710-T-C

47323990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104576756-G-A

47323990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104576756-G-C

47323990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104576756-G-T

http://identifiers.org/hco/17/GRCh38#47323999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#104576765-C-A

47324004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 104576770-G-C

47324004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 104576770-G-T

47324016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 104576782-G-A

47324016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 104576782-G-T

47324097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104576880-G-T

47324098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104576881-A-G

47324098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104576881-A-T

47324110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104576888-G-T

http://identifiers.org/hco/17/GRCh38#47324123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#104576901-C-A

47324123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 104576901-C-T

47324142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104576921-G-A

47324142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104576921-G-T

47324186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 104576957-G-A

47324186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 104576957-G-T

47324220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 104576991-G-A

47324220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 104576991-G-T

47324399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 104577107-T-C

47324581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104577260-C-T

47327035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104577407-T-C

47328009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104578017-A-G

47328026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104578041-T-G

47328238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104578259-G-A

47328238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104578259-G-T

47328296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104578369-A-G

47328296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104578369-A-T

47328450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104578548-C-G

47328450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104578548-C-T

47328517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104578611-T-A

47335168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104581658-G-A

47335254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 104581745-C-G

http://identifiers.org/hco/17/GRCh38#47335416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104581910-A-C

47335420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104581914-T-A

47335517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104581990-A-G

47335553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104582034-C-T

47335568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104582049-A-G

47337192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104582856-C-T

47337565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104582994-T-A

47338142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104583106-T-C

47338187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104583159-G-A

47338558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104583207-G-A

47338558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104583207-G-T

47338600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104583249-A-G

47338642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104583283-A-G

47338794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104583457-A-G

47338806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104583468-G-A

http://identifiers.org/hco/17/GRCh38#47341984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104584202-A-C

47341984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104584202-A-G

47342040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104584261-A-G

47343626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104589175-C-T

47343736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104589281-G-T

47344054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104589605-G-A

47344054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104589605-G-T

47344066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104589617-T-C

47344145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104589691-C-T

47344362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104589890-T-C

47344484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104590003-T-C

47344597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104590402-C-T

47344684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104590493-T-C

47344945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104591349-T-A

47344945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104591349-T-G

47345000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104591420-G-A

47345000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104591420-G-T

http://identifiers.org/hco/17/GRCh38#47346014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104592188-C-A

47346061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104592216-A-G

47346087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104592239-C-G

47346087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104592239-C-T

47346203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104592347-A-G

47346224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104592368-C-T

47346422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104592589-T-A

47346422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104592589-T-C

http://identifiers.org/hco/17/GRCh38#47346424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104592591-A-C

47346424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104592591-A-G

http://identifiers.org/hco/17/GRCh38#47346425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104592592-C-A

47346425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104592592-C-T

47346453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104592610-G-A

47346453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104592610-G-C

47346453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104592610-G-T

47346538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104592690-T-C

47347723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104595047-G-A

47347723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104595047-G-T

47347724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104595048-A-G

47347724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104595048-A-T

47347725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104595049-T-A

47347725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104595049-T-G

47347800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104595118-G-A

47347800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104595118-G-T

http://identifiers.org/hco/17/GRCh38#47347805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104595123-C-A

47347805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104595123-C-T

http://identifiers.org/hco/17/GRCh38#47347903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104595221-A-C

47347903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 104595221-A-G

http://identifiers.org/hco/17/GRCh38#47348015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104595321-A-C

47348036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104595345-A-G

47348054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104595351-T-C

47348096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104595371-T-C

47348117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104595391-A-G

http://identifiers.org/hco/17/GRCh38#47348276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104595555-C-A

47348383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104595665-T-A

47349536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104597575-C-T

47349596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104597658-T-A

47350529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104599295-T-G

47350548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104599316-A-G

47350577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104599346-G-A

47361325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104601342-C-G

http://identifiers.org/hco/17/GRCh38#47361331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104601348-C-A

47361331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104601348-C-T

47361357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104601374-A-G

47361466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104601495-T-C

47361488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104601517-T-C

47361488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104601517-T-G

47361502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104601531-A-G

47361508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104601537-T-C

47361643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104601630-T-A

47361643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104601630-T-C

47361672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104601661-T-C

47363999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104603071-A-G

47364120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104603197-G-A

47370001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104605071-T-C

47370001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104605071-T-G

47370099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104605166-A-G

47370099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104605166-A-T

47370299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104605356-A-G

47370299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104605356-A-T

47370338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104605394-T-C

http://identifiers.org/hco/17/GRCh38#47370349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104605405-C-A

47370495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104605556-G-A

47370591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104605652-A-G

http://identifiers.org/hco/17/GRCh38#47370689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104605746-A-C

47373054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104609506-A-G

47373130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104609584-G-A

47373130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104609584-G-T

http://identifiers.org/hco/17/GRCh38#47373381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104609815-A-C

47373381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104609815-A-G

47374354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104610977-A-G

47374354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104610977-A-T

47374392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104611015-A-T

47374506-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104611113-T-A

47374506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104611113-T-C

47374581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104611185-C-G

47374605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104611209-G-C

http://identifiers.org/hco/17/GRCh38#47374623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104611227-C-A

47374623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104611227-C-G

47374623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104611227-C-T

http://identifiers.org/hco/17/GRCh38#47374657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104611264-C-A

47374657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104611264-C-G

47374834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104612260-A-G

47374858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104612284-A-G

http://identifiers.org/hco/17/GRCh38#47374920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104612343-C-A

47374998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104612424-A-G

47375971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104613093-C-T

47376150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104613731-T-C

47376150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104613731-T-G

http://identifiers.org/hco/17/GRCh38#47376504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104614190-C-A

47377020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104614757-C-G

47377063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104614800-G-C

47377079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104614816-G-T

47377627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104615202-A-G

47377659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104615231-T-A

47377965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104615495-A-G

http://identifiers.org/hco/17/GRCh38#47377981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104615511-C-A

47377981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104615511-C-T

47378301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104616022-C-T

47378493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104616292-T-C

47378637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104616461-T-C

47379109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104617410-T-A

47379109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104617410-T-C

http://identifiers.org/hco/17/GRCh38#47379137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104617437-C-A

47379137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104617437-C-T

47379216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104617515-T-C

47390396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104618014-G-A

47390557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104619808-T-G

47390776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104620015-A-G

http://identifiers.org/hco/17/GRCh38#47391304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104620387-C-A

47391425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104620505-C-T

47391462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104620542-T-C

47391507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104620587-T-A

47391579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 104620659-T-C

47391579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 104620659-T-G

47393907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104621078-G-A

47393907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104621078-G-C

47393907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104621078-G-T

47394006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104621160-G-T

http://identifiers.org/hco/17/GRCh38#47394018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104621172-C-A

47394018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104621172-C-T

47394050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104621204-A-G

47394052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104621206-T-C

47394059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104621213-T-C

47394106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104621272-A-G

47394116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104621514-T-C

http://identifiers.org/hco/17/GRCh38#47395146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104622733-A-C

47395146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104622733-A-G

47395185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104622773-A-G

http://identifiers.org/hco/17/GRCh38#47395701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104624264-C-A

http://identifiers.org/hco/17/GRCh38#47395790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104624352-C-A

47395790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104624352-C-G

47395790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104624352-C-T

http://identifiers.org/hco/17/GRCh38#47395811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104624374-C-A

47395811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104624374-C-T

47395880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104624445-G-A

47395880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104624445-G-T

47395962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104624527-C-T

http://identifiers.org/hco/17/GRCh38#47395988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104624553-C-A

47396071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104625699-G-A

47396074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104625702-G-T

http://identifiers.org/hco/17/GRCh38#47396149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104625773-A-C

47396222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104625820-G-T

47401092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104626142-G-A

47401182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104626232-T-C

47401299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104626354-A-G

47401420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104626478-G-A

47402190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 104626925-T-A

47402334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104627666-A-G

47402494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104628677-C-T

http://identifiers.org/hco/17/GRCh38#47403975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104629125-A-C

47403987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 104629137-G-A

47404009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, missense_variant
orthologous variants: 104629159-G-C

47404508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104629977-A-T

47407007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104630863-T-G

47407027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104630883-G-A

47407361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104631251-A-T

47407480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104631358-T-A

47407707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104631564-G-A

47408123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104632397-T-C

47409079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104633353-T-C

47409345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104634166-T-C

47409475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104634242-G-A

47409475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104634242-G-T

47409479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104634246-A-G

47409606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104634358-T-C

47409624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104634374-A-G

47409624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104634374-A-T

47409727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104634530-T-C

47411294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104635925-T-G

http://identifiers.org/hco/17/GRCh38#47411370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104636005-C-A

47411370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104636005-C-G

47411370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104636005-C-T

47411389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104636033-C-T

47411624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104636246-G-A

47411667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104636274-T-C

47412981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104637370-G-A

47412981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104637370-G-C

47412981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104637370-G-T

47413030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104637418-G-A

47413030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104637418-G-T

47413050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104637438-G-T

47413702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104638057-C-T

47414631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104640284-T-G

http://identifiers.org/hco/17/GRCh38#47414796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104640420-C-A

47414796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104640420-C-T

47414896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 104640520-G-A

47414896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 104640520-G-T

47416885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104640520-G-T

47416917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104640552-A-G

47416944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104640579-A-G

47428316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104641216-G-A

47428401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104641301-A-G

47429576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104642464-A-G

47429603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104642485-G-A

47429679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104642544-A-T

47429706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104642571-A-G

47429747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104642595-A-G

http://identifiers.org/hco/17/GRCh38#47429839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104642680-C-A

47429839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: missense variant
orthologous variants: 104642680-C-T

47429892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: synonymous variant
orthologous variants: 104642733-T-C

47430020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104642862-G-T

http://identifiers.org/hco/17/GRCh38#47430111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104642945-C-A

47430111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104642945-C-T

47430276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104643098-G-T

47430340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104643158-T-C

47430514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104643275-A-G

http://identifiers.org/hco/17/GRCh38#47438990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104643856-C-A

47439028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: intron variant
orthologous variants: 104643894-T-C

47440452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: missense variant
orthologous variants: 104644703-A-G

47440793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 3 prime UTR variant
orthologous variants: 104651206-G-T

http://identifiers.org/hco/17/GRCh38#47440844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104651261-C-A

47440844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 3 prime UTR variant
orthologous variants: 104651261-C-T

47440864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 3 prime UTR variant
orthologous variants: 104651290-T-C

http://identifiers.org/hco/17/GRCh38#47440866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104651292-C-A

47440866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 3 prime UTR variant
orthologous variants: 104651292-C-T

47440941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 3 prime UTR variant
orthologous variants: 104651367-T-A

47440941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 3 prime UTR variant
orthologous variants: 104651367-T-C

47441031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 3 prime UTR variant
orthologous variants: 104651434-T-C

47441068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 3 prime UTR variant
orthologous variants: 104651467-C-T

http://identifiers.org/hco/17/GRCh38#47441069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26864
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#104651468-C-A