43908674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77245803-T-G

43908807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77245665-A-G

43909025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77245449-G-C

43909263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77245054-T-A

43909312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77245019-A-G

http://identifiers.org/hco/13/GRCh38#43909590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77244768-A-C

43909603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244755-G-T

http://identifiers.org/hco/13/GRCh38#43909743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77244638-A-C

43909893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244508-A-G

43909955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244458-A-T

43910401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244092-G-C

43910412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244083-A-G

http://identifiers.org/hco/13/GRCh38#43910457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77244040-A-C

43910617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243969-A-G

43910617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243969-A-T

43911085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243622-C-G

43911085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243622-C-T

43911160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243556-T-G

43911334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243379-C-T

43911338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243375-A-G

43911535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243163-C-T

43911579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243132-T-C

43911723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77242993-T-G

43911747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77242965-G-C

43911834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77242888-T-C

43911847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77242878-G-A

43912231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77242290-G-A

43912642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77241919-A-G

43913019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77241546-G-A

43913369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77241317-T-C

43913422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77241265-G-T

43913437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77241250-T-A

43914259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77240025-C-T

43914956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77239114-G-A

43914966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77239094-G-A

43915307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77238465-C-T

43917052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77233935-T-C

43917747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77233281-T-C

43917877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77233178-T-G

43917940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77233126-G-A

http://identifiers.org/hco/13/GRCh38#43918368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77232739-A-C

43918397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77232702-G-A

43918522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77232540-G-C

43918615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77232450-G-A

43918875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77232206-A-G

43918955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77232134-C-T

http://identifiers.org/hco/13/GRCh38#43919144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77231960-C-A

43919144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77231960-C-T

43919621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77230003-G-C

43919636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77229988-A-G

43920087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77229317-T-G

43920790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77228681-C-G

43920790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77228681-C-T

43921087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77228430-A-G

43921106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77228411-C-T

43921113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77228404-A-G

43933921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77222464-T-C

43933984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77222398-C-T

43934070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77222231-G-A

43934256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77222064-T-C

43934301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77222021-C-T

43934412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77221914-C-G

43934412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77221914-C-T

43934475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77221886-G-A

43934862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77221548-C-G

http://identifiers.org/hco/13/GRCh38#43935010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77221407-A-C

43935065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77221385-A-G

43935195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77221283-C-T

43935203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77221275-C-G

43935210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77221268-T-G

43935297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77221180-G-A

http://identifiers.org/hco/13/GRCh38#43935488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77220987-A-C

43935615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77220888-C-T

43935841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77220720-A-G

43936003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77220605-G-C

43936263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77220373-T-A

43937866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77218691-T-C

43938049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77218529-C-G

43938151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77218419-A-G

43938373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77218210-T-C

http://identifiers.org/hco/13/GRCh38#43938762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77217822-C-A

43939176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217455-A-G

43939255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217423-C-T

http://identifiers.org/hco/13/GRCh38#43939430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77217249-A-C

43939489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217190-C-T

43939591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217121-C-T

43939617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217096-A-G

43939703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217015-G-A

43939703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217015-G-T

43939809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77216914-T-C

43939857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77216699-T-C

43940036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77216527-A-T

43940122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77216437-G-A

43940189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77216372-C-T

43940421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77216160-A-G

43940532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77216082-G-T

http://identifiers.org/hco/13/GRCh38#43940533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77216081-C-A

43940574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77216048-C-T

43940595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77216027-T-C

43944865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215828-C-T

43944904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215792-T-C

43944909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215787-G-A

43944923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215774-C-T

43945045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215584-C-T

43945150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215494-T-C

http://identifiers.org/hco/13/GRCh38#43945263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77215403-C-A

43945264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215402-C-T

43945718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77214970-T-C

43945834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77214867-T-G

43945874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77214828-A-G

43947670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77212791-G-A

43947708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77212761-A-G

43947866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77212601-A-G

43947866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77212601-A-T

43948312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77212236-G-A

http://identifiers.org/hco/13/GRCh38#43948398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77212166-A-C

43948419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77212145-G-A

43948690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77209432-A-G

43948738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77209394-G-C

43948739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77209393-G-A

43948900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77209211-A-G

43949086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77209019-T-A

43949180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208704-A-G

43949180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208704-A-T

43949588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208372-T-C

43949699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208263-C-T

43949719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208243-T-C

43949936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208111-G-A

43950122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77207891-G-T

43950173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77207840-T-G

43950764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77207080-A-G

43950973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77206776-G-A

43951053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77206698-T-C

43957882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77205133-G-A

43957882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77205133-G-T

43957901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77205115-G-A

43957956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77205055-A-G

43959036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77202555-A-G

43959242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77202348-T-G

43959260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77202331-T-G

43959266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77202325-T-A

43959284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77202307-T-C

43959347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77202266-T-A

43959419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77202192-A-G

43959576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77202062-A-G

http://identifiers.org/hco/13/GRCh38#43959686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77201951-A-C

43959846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201803-G-A

43960222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201734-C-T

43960871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77199928-G-T

43960979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77199864-A-T

http://identifiers.org/hco/13/GRCh38#43961194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77199662-C-A

43961261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77199599-G-A

43961363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77199496-C-G

43961742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77199307-A-G

43962522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198729-T-G

43962822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198447-A-G

43962878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198417-A-G

43963044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198317-G-C

43963426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198067-C-T

43963636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197911-G-A

43963891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197716-A-T

43963976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197629-C-G

43964042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197575-A-G

43964144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197504-A-G

43964169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197475-G-T

43964205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197397-A-G

43964213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197389-T-G

43964216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197386-G-C

43964422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197010-G-A

43964749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196693-C-G

43964947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196499-T-C

43964975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196472-G-T

43965810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195553-A-G

43965917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195203-G-A

43965917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195203-G-T

43966022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195106-A-G

43977383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194348-A-G

43977615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194184-G-T

43977626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194173-T-C

http://identifiers.org/hco/13/GRCh38#43977677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77194169-C-A

43977677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194169-C-T

43977678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194168-C-T

http://identifiers.org/hco/13/GRCh38#43977681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77194165-C-A

43977681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194165-C-T

43977685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194161-C-T

43977689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194157-C-T

43977693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194153-T-C

43977693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194153-T-G

43977695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194151-C-T

43977696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194150-T-C

43977697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194149-T-A

43977697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194149-T-C

43977699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194147-C-T

43977700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194146-T-C

43977701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194145-T-A

43977701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194145-T-C

43977701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194145-T-G

43977703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194143-C-G

43977703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194143-C-T

43977705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194141-C-T

43977788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194118-T-C

43977861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194074-T-C

43977901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194048-C-T

43977912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194037-T-G

43978090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77193935-T-C

43978235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77193803-C-G

43979250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77192760-C-T

43979406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77192599-A-G

43979474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77192551-A-G

http://identifiers.org/hco/13/GRCh38#43979916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77192116-C-A

43979916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77192116-C-G

43979982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77192056-A-G

43979996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77192042-T-A

43979996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77192042-T-C

43980243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77191854-T-C

43980246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77191851-G-A

43980643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77191435-A-G

43980843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77191258-G-A

43981029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77191080-A-G

43981029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77191080-A-T

43981435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77190989-C-T

43981600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77190826-G-A

43981709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77190724-G-T

43981765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77190667-T-C

43981846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77190594-C-G

43981846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77190594-C-T

http://identifiers.org/hco/13/GRCh38#43981994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77190452-C-A

43982039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77190399-T-C

43982042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77190396-C-G

43982525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77190027-T-A

43982532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77190020-A-T

43982764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77189795-G-T

43982831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77189726-A-T

43982908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77189648-G-A

http://identifiers.org/hco/13/GRCh38#43983079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77189487-A-C

43983092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77189479-T-G

43983109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77189462-C-T

43983133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77189438-T-C

43983824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77188628-C-T

43984175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77188247-G-A

43984181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77188241-T-C

43984437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77187984-T-C

43984574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77187846-C-G

43984574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77187846-C-T

43984763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77187684-A-G

43984763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77187684-A-T

43984774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77187673-A-G

43985179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77187340-T-C

43985362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77187175-A-T

43985396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77187141-G-A

43985534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77187037-T-G

43985866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77186732-C-T

43985898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77186699-A-G

43985979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77186622-T-C

43986669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77185935-T-C

43986762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77185874-T-C

43986834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77185815-T-C

43988707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77183279-C-T

43988955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77183032-C-T

43988982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77183005-G-A

43989435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77182486-T-C

http://identifiers.org/hco/13/GRCh38#43989448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77182474-A-C

43989651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77182272-G-C

43989704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77182220-C-G

43991028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77174752-G-A

43991077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77174698-T-C

http://identifiers.org/hco/13/GRCh38#43991167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77174607-C-A

43991237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77174535-A-G

43991882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77173157-A-G

43991892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77173147-G-A

43991923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77173116-C-T

43991979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77173060-G-A

43991979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77173060-G-C

43992007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77173032-T-C

43992016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77173023-C-T

43992214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77172844-T-C

43992468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77172661-A-T

43992547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77172471-T-A

43992547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77172471-T-C

43992714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77172314-G-A

43993004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77171074-T-G

43994318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77170932-G-T

43994355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77170892-G-C

43994617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77170660-C-T

43994650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77170626-C-T

43995154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77170195-G-A

http://identifiers.org/hco/13/GRCh38#43996049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77170043-A-C

43996067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77170025-T-C

43996080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77170012-A-G

43996084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77170008-C-T

43996237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77169862-G-A

43996287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77169833-C-T

43996341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77169779-T-C

43996373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77169747-C-G

43996500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77169369-A-G

43996500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77169369-A-T

43996619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77169225-C-G

43997939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77168001-C-G

43997939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77168001-C-T

43997945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77167995-T-C

43998297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77166119-C-G

43998356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77166044-G-A

43998356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77166044-G-C

44002287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77165341-A-G

44002501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77165160-A-G

44002559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77165106-G-A

44002694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77164976-C-G

44002703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77164967-T-G

44002759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77164906-G-A

44002981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77164709-T-G

44003238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77164467-G-T

44003255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77164450-G-T

44003321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77164387-C-T

44004685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77163490-A-G

44004884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77163306-A-G

http://identifiers.org/hco/13/GRCh38#44005038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77163185-C-A

44005038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77163185-C-T

http://identifiers.org/hco/13/GRCh38#44005112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77163120-A-C

44005157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77163086-T-A

44005209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77163035-G-T

44005237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77163012-T-G

44005496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77162796-A-G

44005674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77162601-A-G

44007157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77160672-T-C

44007321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77160504-G-A

44007338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77160487-T-G

44007391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77160439-C-G

44007495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77160327-T-G

http://identifiers.org/hco/13/GRCh38#44007527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77160294-C-A

http://identifiers.org/hco/13/GRCh38#44007676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77160142-C-A

44007722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77160096-A-G

44007815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77160004-G-T

44007946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77159893-T-C

44007994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77159846-C-T

44008240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77159602-C-T

44008603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77159266-G-A

44008628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77159241-T-G

44008631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77159238-T-C

44008731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77159143-T-C

44009307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77158567-T-C

44009596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77158241-T-C

44009663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77158174-T-G

44010019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77157876-T-A

44010246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77157687-C-T

44010571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77157397-A-G

44010863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77157135-G-A

http://identifiers.org/hco/13/GRCh38#44012432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77156288-A-C

44012432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77156288-A-G

http://identifiers.org/hco/13/GRCh38#44012494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77156255-A-C

44012494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77156255-A-G

44012494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77156255-A-T

44012505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77156244-T-C

44012630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77156108-T-C

44012748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77155997-A-G

44012908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77155851-C-T

44013798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77154965-G-A

http://identifiers.org/hco/13/GRCh38#44013900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77154876-A-C

44013900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77154876-A-G

44013919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77154857-C-G

44013919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77154857-C-T

44014099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77154704-C-G

44014434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77154366-G-C

44014598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77154191-C-G

http://identifiers.org/hco/13/GRCh38#44014881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77153563-C-A

44015288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77153222-C-G

44015295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77153215-G-C

44015647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77152848-G-A

http://identifiers.org/hco/13/GRCh38#44015848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77152650-C-A

44015872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77152626-G-C

44016864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77151523-A-G

44016965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77151439-G-A

44017170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77151281-G-C

44017188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77151263-G-T

44017603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150868-A-G

44017647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150833-C-T

44017700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150790-A-G

http://identifiers.org/hco/13/GRCh38#44017976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77150523-C-A

44017976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150523-C-T

44018039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150458-A-G

44018167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150343-G-A

44018447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150080-C-T

44018523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150005-A-G

44018549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77149989-C-T

44019114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77148254-C-G

44019182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77148193-G-A

44019185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77148190-A-G

44019202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77148173-T-C

44019369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77148006-G-A

44019773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77147493-A-G

44019798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77147468-G-A

44019806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77147460-C-T

44019911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77147397-A-G

44020064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77147240-A-G

44020079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77147225-C-T

44020290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77147012-C-T

44020438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77146867-C-T

44020784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77146621-T-C

44020786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77146619-A-G

44020811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77146594-T-G

44021549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77145828-G-T

44021581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77145796-T-C

44021687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77145691-T-G

http://identifiers.org/hco/13/GRCh38#44022241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77145110-C-A

44022310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77145046-C-T

http://identifiers.org/hco/13/GRCh38#44022326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77145030-C-A

44022370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77144987-G-T

44022429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77144929-G-A

44022429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77144929-G-T

44022445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 77144913-G-T

44022592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77144768-A-G

44022606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77144754-G-A

44022946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77142538-C-G

44023021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77142467-A-T

44023111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77142368-G-A

44023119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77142360-T-C

44023792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77141945-G-A

44023904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77141852-G-T

44023941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77141812-C-T

44023956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77141797-C-T

44024045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77141736-T-C

44024248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77141576-C-T

44024544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77141334-A-G

44024937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77140801-A-G

44025257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77140526-T-A

44025300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77140484-G-T

44025359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77140426-T-C

44025400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77140381-T-C

http://identifiers.org/hco/13/GRCh38#44025439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77140341-C-A

44025439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77140341-C-T

44025465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77140315-T-C

44025465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77140315-T-G

44025476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77140304-T-C

44025550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77140231-G-T

44025572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77140211-G-C

44025599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77140187-T-C

http://identifiers.org/hco/13/GRCh38#44025601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77140185-C-A

44025601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77140185-C-G

44025639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77140149-G-T

http://identifiers.org/hco/13/GRCh38#44025652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77140136-C-A

44025652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77140136-C-T

44025660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77140128-C-T

44025780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77140051-C-T

44025874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77139962-T-C

44025900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77139936-G-A

44026061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77139786-G-A

44026061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77139786-G-T

44026097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77139749-T-A

44026151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77139705-T-C

http://identifiers.org/hco/13/GRCh38#44026345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77139500-C-A

44026345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77139500-C-T

http://identifiers.org/hco/13/GRCh38#44026399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77139444-C-A

44026492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77138960-G-A

http://identifiers.org/hco/13/GRCh38#44026566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77138891-C-A

44026566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77138891-C-T

http://identifiers.org/hco/13/GRCh38#44026573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77138884-C-A

44026573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77138884-C-G

44026583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77138875-A-G

44026589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77138869-A-G

44026604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77138854-G-T

44026615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77138843-T-A

44026690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77138775-A-G

http://identifiers.org/hco/13/GRCh38#44026861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77138609-C-A

44026861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77138609-C-T

44026867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77138603-G-A

44026927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77138543-G-T

http://identifiers.org/hco/13/GRCh38#44026993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77138496-C-A

44026993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77138496-C-T

44027042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77138449-G-T

44027091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77138388-G-A

44027092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77138387-G-T

44027152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77138328-A-G

44027282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77138208-G-A

http://identifiers.org/hco/13/GRCh38#44027424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77138070-A-C

44027424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77138070-A-G

44027598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77137909-G-A

44027637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77137867-T-C

http://identifiers.org/hco/13/GRCh38#44027679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77137826-A-C

44027805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77137712-A-G

http://identifiers.org/hco/13/GRCh38#44027877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77137641-C-A

44027936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77137594-G-A

44028306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 77137214-T-C

44028445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77137082-G-T

http://identifiers.org/hco/13/GRCh38#44028447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77137078-C-A

44028447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77137078-C-T

44028455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77137070-G-T

http://identifiers.org/hco/13/GRCh38#44028493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77137034-C-A

44028515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77137002-T-C

44028533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136984-G-T

44028537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136980-G-A

44028537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136980-G-T

44028581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136929-A-G

44028647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136866-T-C

44028650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136863-A-G

44028677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136838-G-A

44028714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136795-G-T

http://identifiers.org/hco/13/GRCh38#44028737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77136772-C-A

44028737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136772-C-T

44028793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136719-G-T

44029153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136393-G-A

44029153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136393-G-T

44029159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136387-A-G

44029195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136351-C-T

44029362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136288-G-T

44029386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136264-A-G

44029397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136255-A-G

44029448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136206-A-G

44029463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136191-G-A

44029463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136191-G-T

44029512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136147-T-C

44029547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136129-G-A

44029634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77136049-A-G

44029672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77135968-T-C

44029683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77135957-C-T

44029687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77135953-T-C

http://identifiers.org/hco/13/GRCh38#44029700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77135931-C-A

44029796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77135835-C-T

44029798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77135833-G-A

44029798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77135833-G-T

44029850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77135771-T-C

44029867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77135754-G-A

44029867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77135754-G-T

44029944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77133702-T-C

44030067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77133569-G-T

44030178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77133451-A-G

44030347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26981
most severe consequence: non coding transcript exon variant
orthologous variants: 77133315-A-G