55846168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 94225705-T-G

55846335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 94225896-A-G

55846336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 94225897-G-A

55846336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 94225897-G-C

55846336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 94225897-G-T

55846375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 94225935-G-A

55846375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 94225935-G-C

55846375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 94225935-G-T

55846411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 94225971-G-A

55846411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 94225971-G-T

http://identifiers.org/hco/16/GRCh38#55846437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94225993-A-C

55846437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 94225993-A-G

55846462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94226017-A-G

55846508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94226063-A-G

55846540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94226095-G-A

55846540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94226095-G-T

55846643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94226198-A-G

55846663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94226218-G-A

55846700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94226255-A-G

http://identifiers.org/hco/16/GRCh38#55846702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94226257-C-A

55846702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94226257-C-T

55846770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 94226318-G-A

55846770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 94226318-G-T

55846866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94226414-G-A

55846866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94226414-G-T

55846899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94226443-G-T

http://identifiers.org/hco/16/GRCh38#55846966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94226454-C-A

55846966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94226454-C-T

55846968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94226456-G-A

55846968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94226456-G-T

55847009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94226466-C-G

http://identifiers.org/hco/16/GRCh38#55847185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94226617-A-C

55847185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94226617-A-G

55847258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94226701-C-T

55847274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94226721-C-T

http://identifiers.org/hco/16/GRCh38#55847282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94226729-C-A

55848474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94227886-C-T

http://identifiers.org/hco/16/GRCh38#55848552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94227970-A-C

55848738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94228136-G-C

55848801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94228191-T-C

55848839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94228224-T-G

55848933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94228367-T-C

55848992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94228418-A-G

55849602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94228777-T-A

55849602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94228777-T-C

55849700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94228882-A-G

55849834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94228997-T-C

http://identifiers.org/hco/16/GRCh38#55849842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94229005-C-A

55849842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94229005-C-G

55849870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94229032-G-A

55849870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94229032-G-T

http://identifiers.org/hco/16/GRCh38#55849902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94229122-C-A

http://identifiers.org/hco/16/GRCh38#55852805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94240753-C-A

55852805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94240753-C-T

55852822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94240770-T-C

55852822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94240770-T-G

55852849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94240791-A-G

55853074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94241128-G-T

55853092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94241150-C-G

55853428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94241429-C-T

55853700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94241677-C-T

55853801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94241772-G-C

55853951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94241933-C-G

55853986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94241968-G-A

55854118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94242095-A-G

55854130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94242104-A-T

55854148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94242122-C-G

http://identifiers.org/hco/16/GRCh38#55854155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94242129-C-A

55854155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94242129-C-T

55854288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94242255-C-T

55854349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94242345-T-C

55854724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94242542-G-T

55855326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94242947-G-A

55856272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94243429-G-A

55856272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94243429-G-T

http://identifiers.org/hco/16/GRCh38#55856303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94243460-C-A

55856303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94243460-C-T

http://identifiers.org/hco/16/GRCh38#55856562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94243716-C-A

55856562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94243716-C-T

http://identifiers.org/hco/16/GRCh38#55856571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94243725-C-A

55856571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94243725-C-T

55856590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94243744-A-G

http://identifiers.org/hco/16/GRCh38#55857123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94244242-C-A

55857167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94244279-G-C

55857289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94244396-T-C

55857289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94244396-T-G

55857317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94244424-A-G

55857406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94244509-A-G

55857556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94244573-C-T

55857560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94244577-A-G

55857683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94244647-G-A

55857748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94244730-A-G

http://identifiers.org/hco/16/GRCh38#55858688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94244956-C-A

55858688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94244956-C-G

55858911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94245171-C-G

55859411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94246012-G-A

55859411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94246012-G-T

55859527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94246112-T-C

55859658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94246243-A-G

55859694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 94246279-T-A

55859694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 94246279-T-C

http://identifiers.org/hco/16/GRCh38#55859741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94246314-C-A

55859741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94246314-C-T

http://identifiers.org/hco/16/GRCh38#55859742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94246315-A-C

55859816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94246358-A-G

55859845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94246394-A-G

55860389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94246574-A-G

55860548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94246704-T-C

55860563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94246743-T-G

55860665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94246903-G-A

55860759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94246994-C-T

55860937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94247157-T-G

http://identifiers.org/hco/16/GRCh38#55861217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94247397-C-A

http://identifiers.org/hco/16/GRCh38#55861228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94247408-C-A

55861228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94247408-C-T

http://identifiers.org/hco/16/GRCh38#55861291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94247469-A-C

http://identifiers.org/hco/16/GRCh38#55861364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94247553-C-A

55861364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94247553-C-T

55861372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94247560-A-G

55861510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 94247696-C-T

55861576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94247756-A-G

55861594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94247773-A-G

http://identifiers.org/hco/16/GRCh38#55861595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94247774-A-C

55861595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94247774-A-G

55861630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94247808-T-A

55861936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94247997-A-G

55861936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94247997-A-T

55862004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94248050-C-T

55862343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94248371-G-T

55862349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94248377-G-A

55862412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94248433-T-A

http://identifiers.org/hco/16/GRCh38#55862542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94248564-A-C

55862590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94248615-T-C

55862599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94248624-A-G

55862907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94249044-T-C

55863185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94249301-T-G

55863247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94249662-A-G

55863247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94249662-A-T

55863274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94249689-G-A

55863274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94249689-G-T

55863469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94249873-G-A

55863469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94249873-G-T

55863525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94249931-A-G

55863594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94249996-T-C

55863847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94250100-C-T

http://identifiers.org/hco/16/GRCh38#55864109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94250276-C-A

55864109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94250276-C-T

55864609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94250906-G-A

55865712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94251678-G-A

55865811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94251781-C-G

55865855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94252007-T-C

http://identifiers.org/hco/16/GRCh38#55865882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94252083-C-A

55865882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94252083-C-T

http://identifiers.org/hco/16/GRCh38#55865918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94252128-C-A

55865918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94252128-C-T

55865950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94252161-G-A

55865994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 94252205-T-A

55865999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 94252210-A-G

55866200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94252417-G-A

55866200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94252417-G-T

55866208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94252425-T-A

55866208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94252425-T-C

55866208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94252425-T-G

55867477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94254042-A-G

55867522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94254083-T-C

55867751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94254278-C-G

http://identifiers.org/hco/16/GRCh38#55867909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94254411-C-A

http://identifiers.org/hco/16/GRCh38#55867970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94254481-C-A

55869183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94254727-C-T

55869219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94254764-C-T

55869245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94254790-C-G

55869245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94254790-C-T

http://identifiers.org/hco/16/GRCh38#55869371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94254905-C-A

55869371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94254905-C-T

http://identifiers.org/hco/16/GRCh38#55869394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94254928-A-C

55869394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94254928-A-T

55869449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94254976-G-A

55869449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94254976-G-T

55869453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94254980-T-A

55869480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 94255005-T-C

55869483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255008-G-A

55869483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255008-G-T

55869522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255047-G-A

55869522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255047-G-T

55869540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255065-G-T

http://identifiers.org/hco/16/GRCh38#55869561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94255080-C-A

55869561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255080-C-T

55869563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255082-C-T

55869585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255103-G-A

55869585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255103-G-T

55869754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255269-G-A

55869754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255269-G-C

55869754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255269-G-T

55869892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255406-G-A

55869892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255406-G-T

55869914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255429-C-T

55869915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255430-C-T

55869925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255440-C-T

55869999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255499-C-T

55870477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94255990-G-T

55870978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94256583-G-A

55871008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94256612-C-T

55871009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94256613-G-A

55871161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94256751-G-A

55871345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94256938-G-C

55871367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94256959-G-A

55871367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94256959-G-C

55871502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94257094-T-A

55871502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94257094-T-C

55871502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94257094-T-G

55871531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94257306-G-A

55871531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94257306-G-T

55871535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94257311-G-A

55871535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94257311-G-C

55871535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94257311-G-T

55871576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94257333-G-A

55871583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94257350-T-A

55871652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 94257414-G-A

http://identifiers.org/hco/16/GRCh38#55871854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94257636-C-A

55871854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94257636-C-T

55871877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94257653-G-A

55871877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94257653-G-C

55871877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94257653-G-T

http://identifiers.org/hco/16/GRCh38#55871927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94257705-C-A

55871927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94257705-C-T

http://identifiers.org/hco/16/GRCh38#55871932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94257710-C-A

55871932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94257710-C-T

55871943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94257721-G-A

55872249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94257941-C-T

55872346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94258031-A-G

55872452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94258137-C-T

55872543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94258229-C-G

55872835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94258607-A-G

55872878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94258635-C-T

55872962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94259247-A-T

55873030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94259345-T-C

55873032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94259347-G-C

55873052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94259367-G-A

55873401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94260573-A-G

55873411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94260583-C-T

55873688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261001-C-T

55873694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261007-A-T

http://identifiers.org/hco/16/GRCh38#55873730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94261039-C-A

55873730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261039-C-T

55873782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261084-C-G

55873782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261084-C-T

55873973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 94261276-A-G

55873976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 94261279-G-C

55874044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 94261347-G-A

55874044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 94261347-G-T

55874056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261359-G-A

55874056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261359-G-T

55874058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261361-A-G

55874072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261375-T-C

55874080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261383-G-T

55874104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261402-T-C

55874104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261402-T-G

55874151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261434-G-A

55874151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261434-G-C

55874151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261434-G-T

55874156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261439-T-C

55874178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261450-T-C

55874225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261493-C-G

55874225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261493-C-T

http://identifiers.org/hco/16/GRCh38#55874325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94261566-C-A

55874325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261566-C-T

55874383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261610-A-T

55874575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261791-G-A

55874608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261829-A-G

55874736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261961-G-A

55874762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94261972-A-G

55874892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94262096-G-A

55875052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94262161-C-T

55875057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94262171-G-A

55875160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 94262274-G-T

55875169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 94262283-A-G

55875230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94262345-C-T

55875243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94262358-G-C

55875260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94262375-C-T

55875266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94262381-G-A

55875299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94262414-G-A

http://identifiers.org/hco/16/GRCh38#55875315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94262430-C-A

55875315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94262430-C-T

55875341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94262457-A-G

http://identifiers.org/hco/16/GRCh38#55875350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94262466-A-C

55875350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94262466-A-G

http://identifiers.org/hco/16/GRCh38#55875363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94262479-A-C

55875363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94262479-A-G

http://identifiers.org/hco/16/GRCh38#55875370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94262486-C-A

http://identifiers.org/hco/16/GRCh38#55875390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94262505-A-C

55875445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94262563-A-G

55875445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94262563-A-T

55875456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94262574-G-A

55875456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94262574-G-T

55875466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94262583-T-C

55875474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94262590-G-C

55875474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94262590-G-T

55899527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94288939-C-T

55899969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94288991-T-G

http://identifiers.org/hco/16/GRCh38#55900074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94289093-C-A

55900196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94289184-G-A

55900284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94289273-T-C

55900298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94289287-G-T

55900415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94289416-T-C

55900473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94289475-G-A

55900526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94289529-G-C

55900542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94289547-G-A

55900579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94289583-T-C

55900630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94289633-G-A

55900630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94289633-G-C

55900630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94289633-G-T

55900721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94289689-C-T

55900798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94289760-T-C

55900928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94289898-A-G

55901530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94290247-T-C

55901530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94290247-T-G

55901551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94290270-C-G

55901752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94290439-T-C

55901837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94290522-T-C

55901880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94290565-T-C

http://identifiers.org/hco/16/GRCh38#55901977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94290651-C-A

55901977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94290651-C-T

55902203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94290847-T-C

55902203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94290847-T-G

55902214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94290858-A-G

55902333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94290982-C-T

55902768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94291343-C-G

55902846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94291414-G-A

55902914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94291465-T-C

http://identifiers.org/hco/16/GRCh38#55903009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94291550-C-A

55903009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94291550-C-T

55903083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94291632-G-A

55903121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94291666-G-A

55903121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94291666-G-T

55903129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94291674-G-A

55903188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94291731-C-G

55903207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94291751-T-C

55903351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94291873-G-T

55904902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94292580-A-T

55905049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94292718-T-C

55905192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94293203-A-G

55905276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94293235-G-A

55905334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94293302-G-A

55905338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94293306-T-A

http://identifiers.org/hco/16/GRCh38#55905345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94293313-A-C

55905345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94293313-A-T

55905690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94293341-C-G

55905690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94293341-C-T

http://identifiers.org/hco/16/GRCh38#55905709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94293347-C-A

55905712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94293350-G-A

55905752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94293401-G-C

55905752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94293401-G-T

55905787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94293436-A-G

55906234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94293835-G-A

55906451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94294053-A-G

55906563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94294159-G-A

55906693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94294251-A-G

55909064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94294520-G-A

55909121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94294578-G-A

55909211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94294667-G-A

55909410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94294876-C-T

http://identifiers.org/hco/16/GRCh38#55910872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94295180-C-A

55911201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94295518-G-A

55911296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94295600-G-A

http://identifiers.org/hco/16/GRCh38#55911504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94295796-A-C

55911865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94296147-C-T

55911991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94296240-T-C

55912108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94296396-T-C

55912297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94296588-C-T

55912377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94296667-G-A

55912377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94296667-G-C

55913847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94297523-A-G

55913931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94297601-G-A

55914154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94297811-G-T

55914268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94297886-T-C

http://identifiers.org/hco/16/GRCh38#55914926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94298576-A-C

55915077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94298730-A-G

55915088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94298738-T-C

55915145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94298797-C-G

55915145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94298797-C-T

55915403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94299057-T-G

55929172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94302443-A-G

55929356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94302614-C-G

55929383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94302645-G-A

55929391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94302653-G-A

55934233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94311091-A-G

55934331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94311191-G-T

55934365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94311225-T-C

55934365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94311225-T-G

55934456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94311285-G-T

55934482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94311311-T-C

55934523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94311350-A-G

55934607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94311413-T-C

55934738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94311529-A-T

55934848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94311646-G-C

55934852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94311651-G-A

http://identifiers.org/hco/16/GRCh38#55935293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94311725-C-A

55935459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94311843-A-G

55935518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94311898-T-C

55935541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94311920-C-T

55935753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94312119-T-C

55935790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94312160-T-C

55935790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94312160-T-G

55935815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94312185-C-T

55935873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94312247-C-T

55936034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94312394-G-C

55936213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94312532-G-A

55936381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94312646-G-A

55936427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94312693-C-G

55936427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94312693-C-T

55936483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94312745-A-T

55936714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94313356-C-G

55936844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94313729-G-T

55936925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94313793-G-A

55937014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94313882-G-T

55937198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94314064-C-G

55937198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94314064-C-T

55937313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94314175-G-T

55937871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94314533-T-C

55937892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94314553-G-A

55937892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94314553-G-C

55938231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94314886-G-T

55938407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94315014-C-T

55938414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94315021-G-A

55938940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94315185-T-A

55939008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94315245-C-T

55941734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94316489-T-C

55941804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94316555-C-G

55941966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94316754-G-A

55942061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94316845-C-T

http://identifiers.org/hco/16/GRCh38#55942244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94317042-C-A

55942245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94317043-C-T

55942258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94317056-G-T

55942261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94317059-G-A

55942333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94317128-C-T

55942358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94317153-C-T

55942384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94317179-C-T

55942440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94317236-C-T

55942461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94317254-T-C

55943094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94317550-T-C

55943113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94317569-T-C

55943115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94317571-A-G

http://identifiers.org/hco/16/GRCh38#55943337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94317760-A-C

55943404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94317822-A-T

55943412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94317830-G-A

55943412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94317830-G-T

55943450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94317869-T-C

55943496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94317916-A-T

55943499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94317919-G-C

55943630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94318031-A-G

55944020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94318369-G-A

55944020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94318369-G-C

55944020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94318369-G-T

55944126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94318458-A-G

http://identifiers.org/hco/16/GRCh38#55944445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94318630-C-A

55944462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94318647-C-T

http://identifiers.org/hco/16/GRCh38#55944523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94318703-C-A

55944527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94318707-G-A

http://identifiers.org/hco/16/GRCh38#55944578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94318759-C-A

55944834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94319017-A-G

55944835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94319018-A-G

55945093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94319292-T-C

55945337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94319531-G-C

55945388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94319571-G-A

http://identifiers.org/hco/16/GRCh38#55945631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94319813-C-A

55945631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94319813-C-T

55945829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94320003-T-C

55946093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94320259-A-T

55946111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94320280-T-G

55946181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94320347-T-C

55946539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94320827-G-A

55946624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94320911-G-C

http://identifiers.org/hco/16/GRCh38#55946701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94320985-C-A

55946701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94320985-C-T

55952635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94323811-A-G

55952864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94324018-T-C

55952864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94324018-T-G

55953014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94324164-G-A

55953118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94324266-T-C

55953193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94324332-T-C

55953222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94324361-T-C

55953226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94324365-T-C

http://identifiers.org/hco/16/GRCh38#55953227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94324366-C-A

55953227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94324366-C-T

55953329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94324438-G-A

55953329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94324438-G-T

55953556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94324696-A-G

55953596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94324738-G-T

55954260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94324956-G-A

55954717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94325400-T-G

55954832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94325489-G-A

55954873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94325531-C-T

55955018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94325654-G-A

55955018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94325654-G-T

55955041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94325674-G-A

55955217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94325794-C-T

55955559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94326096-A-T

55955560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94326097-A-G

55955573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94326110-G-A

55955573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94326110-G-C

55955635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94326176-T-C

55955640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94326182-C-T

55955692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94326236-C-T

55955703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94326246-T-C

55955747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94326275-G-T

55955759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94326315-T-C

55955768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: intron variant
orthologous variants: 94326324-T-C

55955893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5 prime UTR variant
orthologous variants: 94326437-G-T

http://identifiers.org/hco/16/GRCh38#55955949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94326492-A-C

http://identifiers.org/hco/16/GRCh38#55955970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94326513-C-A

http://identifiers.org/hco/16/GRCh38#55956008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94326551-C-A

55956008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26459
most severe consequence: 5 prime UTR variant
orthologous variants: 94326551-C-T