117143640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100804208-T-C

http://identifiers.org/hco/1/GRCh38#117143654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100804193-C-A

117143680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100804168-C-T

117143862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803890-T-A

117143862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803890-T-C

117143917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803837-T-C

117143988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803766-C-T

117144015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803739-C-T

117144078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803693-C-G

http://identifiers.org/hco/1/GRCh38#117144128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100803660-C-A

117144182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803608-T-C

117144230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803560-T-C

117144252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803539-G-A

http://identifiers.org/hco/1/GRCh38#117144284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100803508-C-A

117144284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803508-C-T

117144305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803488-G-T

117144328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803465-C-T

117144349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803431-A-T

117144382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803400-G-T

117144384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803398-G-A

http://identifiers.org/hco/1/GRCh38#117144438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100803350-C-A

117144480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803308-T-C

117144493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803295-T-C

117144493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803295-T-G

117144504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803285-C-G

117144563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803224-C-T

117144627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803158-T-C

http://identifiers.org/hco/1/GRCh38#117144686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100803096-A-C

117144757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803022-G-A

117144757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803022-G-T

http://identifiers.org/hco/1/GRCh38#117144763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100803016-C-A

117144763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100803016-C-T

117144825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100802954-A-G

117144858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100802921-G-A

117144858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100802921-G-T

117144960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100802861-T-C

117144984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100802837-G-T

117145110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100802734-G-A

117145110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100802734-G-T

117145139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100802705-T-A

117145184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100802660-A-G

http://identifiers.org/hco/1/GRCh38#117145225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100802620-C-A

http://identifiers.org/hco/1/GRCh38#117145271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100802576-C-A

117145338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100802502-G-T

117145509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100802343-G-A

117145602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100802252-G-A

http://identifiers.org/hco/1/GRCh38#117146233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100801670-A-C

117146401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100801500-G-T

117146417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100801485-C-T

117146755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100801178-G-A

117146783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100801150-G-A

http://identifiers.org/hco/1/GRCh38#117146792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#100801141-A-C

117146800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100801133-T-C

http://identifiers.org/hco/1/GRCh38#117147019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#100800621-C-A

117147048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100800605-G-C

117147081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100800575-C-T

117147185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100800484-G-T

117147237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100800431-A-T

117147306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100800357-G-T

117147502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100800175-G-T

117147548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100800129-G-A

117147548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100800129-G-C

117147548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100800129-G-T

http://identifiers.org/hco/1/GRCh38#117147580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100800074-C-A

117147580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100800074-C-G

117147580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100800074-C-T

http://identifiers.org/hco/1/GRCh38#117147633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100800015-C-A

117147633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100800015-C-G

117147633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100800015-C-T

117147644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100800004-G-T

http://identifiers.org/hco/1/GRCh38#117147651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100799997-A-C

117147651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100799997-A-T

117147653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100799995-G-C

117147653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100799995-G-T

http://identifiers.org/hco/1/GRCh38#117147691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100799957-A-C

http://identifiers.org/hco/1/GRCh38#117147692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100799956-A-C

117147706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100799942-G-A

117147743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100799902-T-C

117147748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100799897-C-T

117147761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100799884-C-G

117147761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100799884-C-T

117147847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100799804-G-C

117147847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100799804-G-T

117147875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100799779-A-T

117147877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100799777-A-G

117147878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100799776-A-G

http://identifiers.org/hco/1/GRCh38#117147910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100799744-C-A

117147910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100799744-C-G

http://identifiers.org/hco/1/GRCh38#117147911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100799743-C-A

117148117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100799543-G-A

117148334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100799377-T-C

117148343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100799368-T-C

http://identifiers.org/hco/1/GRCh38#117148457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100799292-A-C

117148457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100799292-A-G

http://identifiers.org/hco/1/GRCh38#117152443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100796867-C-A

117152629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100796686-A-G

http://identifiers.org/hco/1/GRCh38#117152744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100796578-C-A

117152790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100796533-G-A

117152836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100796486-C-T

http://identifiers.org/hco/1/GRCh38#117152850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100796440-A-C

117153058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100795874-A-G

117153064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100795869-T-A

117153064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100795869-T-C

117153108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100795739-C-T

117153126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100795721-T-C

117153258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100795589-T-G

117153339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100795508-T-C

117153339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100795508-T-G

117153428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100795354-G-A

117153428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100795354-G-C

117153428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100795354-G-T

117153657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100795045-A-G

117153785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100794898-G-A

117153841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100794844-T-C

http://identifiers.org/hco/1/GRCh38#117154829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100793084-C-A

117154829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100793084-C-T

117155264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100792750-T-G

117155399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100792628-T-G

117155586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100792464-C-G

117155628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100792416-C-G

117156066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100792025-T-C

117156455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100791542-A-G

117156455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100791542-A-T

117156551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100791429-A-G

http://identifiers.org/hco/1/GRCh38#117156553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100791427-C-A

117156603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100791377-C-T

117156702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100791278-T-A

117156849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100791131-G-T

http://identifiers.org/hco/1/GRCh38#117156970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100791015-C-A

http://identifiers.org/hco/1/GRCh38#117157157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100790851-C-A

117157157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100790851-C-G

117157157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100790851-C-T

117157278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100790711-T-C

117159789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100790466-T-A

117159882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100790378-T-C

117160132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100790150-A-G

117160286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100790013-G-A

117160378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100789940-T-C

117160378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100789940-T-G

117160622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100789711-T-G

117160701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100789644-T-C

117160908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100789462-C-T

117161005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100789368-T-C

http://identifiers.org/hco/1/GRCh38#117161080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100789291-C-A

117161245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100789151-C-T

http://identifiers.org/hco/1/GRCh38#117161321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100789071-C-A

http://identifiers.org/hco/1/GRCh38#117162055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100788374-A-C

117162496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100788047-T-C

117162503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100788040-T-C

117162788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100786699-T-C

117163009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100786493-T-C

117163036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100786467-G-A

117163042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100786461-C-T

117163074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100786430-C-T

117163086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100786414-G-T

117163101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100786395-G-A

117163101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100786395-G-T

117163112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100786384-C-T

117163125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100786371-G-A

117163148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100786351-C-T

117163184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100786317-A-G

117163643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100785890-G-A

117163643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100785890-G-T

117164510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100785194-G-A

117164628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100785076-G-C

117164802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100784887-C-G

117169045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100782637-C-G

117169128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100782548-G-A

117169286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100782403-T-C

117170002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100782237-T-C

117170002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100782237-T-G

117170071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100782173-G-A

117170071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100782173-G-T

117170145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 100782101-G-A

http://identifiers.org/hco/1/GRCh38#117170160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#100782086-A-C

117170234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100782012-A-T

http://identifiers.org/hco/1/GRCh38#117170318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#100781941-C-A

117170318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100781941-C-T

http://identifiers.org/hco/1/GRCh38#117170331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#100781928-A-C

http://identifiers.org/hco/1/GRCh38#117170360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#100781368-C-A

117170360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100781368-C-T

117170378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100781351-A-G

117170517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100781218-G-A

117171671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100775950-T-C

117172018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100774573-C-T

117172034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100774557-T-C

117172155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100774452-G-C

http://identifiers.org/hco/1/GRCh38#117172370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100774219-A-C

http://identifiers.org/hco/1/GRCh38#117172378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100774211-C-A

117172610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100774029-C-T

117173926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100772085-T-C

http://identifiers.org/hco/1/GRCh38#117174062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100771943-A-C

117175003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100769419-A-G

117175055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100769379-G-T

http://identifiers.org/hco/1/GRCh38#117175305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100769123-C-A

117175387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100769028-T-C

117175547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100768858-A-G

117175617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100768793-C-T

117176300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100767434-C-T

117176312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100767422-G-T

117176314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100767420-G-A

117176612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100767159-C-G

117176612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100767159-C-T

117176619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100767152-T-C

117176703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100767057-A-T

117177540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100766381-T-C

117177618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100766305-A-G

117178914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100766008-C-T

117179675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100765355-T-C

http://identifiers.org/hco/1/GRCh38#117179945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100765132-A-C

117179960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100765117-G-C

http://identifiers.org/hco/1/GRCh38#117180124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100764981-C-A

117180124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100764981-C-G

117180124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100764981-C-T

117180612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100764535-A-G

117180780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100764410-T-C

117180780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100764410-T-G

117180867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100764334-C-T

http://identifiers.org/hco/1/GRCh38#117181814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#100763661-A-C

117182112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100763395-C-T

http://identifiers.org/hco/1/GRCh38#117182154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100763339-C-A

117182154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100763339-C-T

117182184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100763294-A-G

http://identifiers.org/hco/1/GRCh38#117182312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100762963-C-A

117182312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100762963-C-T

http://identifiers.org/hco/1/GRCh38#117182317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100762958-A-C

117182347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100762933-C-G

117182347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100762933-C-T

117182442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100762839-T-C

117182484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100762796-G-A

117182494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100762781-G-A

117182808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100762491-T-A

117182811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100762488-T-C

117182993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100762274-A-G

117183018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100762246-G-C

117183600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100761677-T-A

117183604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100761673-C-T

117183701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100761576-G-A

117183924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100761166-G-A

117185094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100758176-A-G

117185094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100758176-A-T

117185224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100758071-C-T

117185299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100757995-G-T

117185337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100757955-A-G

117185376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100757920-C-T

117186128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100757794-C-T

117186274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100757660-T-C

http://identifiers.org/hco/1/GRCh38#117186328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100757616-A-C

117186626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100757332-G-A

http://identifiers.org/hco/1/GRCh38#117187345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100756775-C-A

117187375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100756744-C-G

117187375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100756744-C-T

117187582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100756571-T-C

117187963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100756311-A-G

http://identifiers.org/hco/1/GRCh38#117188101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100756168-A-C

117188101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100756168-A-G

117188237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100756024-G-C

117189366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100754351-G-A

117189456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100754303-G-A

117189503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100754265-G-C

117189564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100754222-C-G

117189576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100754210-C-T

117189834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100753977-C-T

117189844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100753967-C-T

117193946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100753776-T-C

117194035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100753699-G-A

117194114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100753621-A-G

117194948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100752583-C-T

117194966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100752573-T-A

117196666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100752072-C-T

117196696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100752046-G-A

117196816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100751931-A-G

117196816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100751931-A-T

117196902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100751848-G-A

117196971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100751789-A-G

117197021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100751739-G-A

117197826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100749092-G-A

117198064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100748898-C-T

117198182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100748794-T-C

117198330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100748702-T-C

117198365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100748668-T-A

117198365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100748668-T-C

117198582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100748440-T-C

117199038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100748009-G-A

117199269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100746826-G-A

117200094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100745395-G-C

117200094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100745395-G-T

117200634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100743713-T-A

117200755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100743610-G-T

117201073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100743296-G-A

117201083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100743259-T-C

http://identifiers.org/hco/1/GRCh38#117201204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100743138-C-A

117201318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100743030-C-T

117201367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100742983-G-A

117201705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100742668-A-T

117202319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100741742-G-A

117202358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100741696-G-A

117202396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100741656-G-C

117202429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100741625-G-C

117202509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100741546-T-G

117202512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100741534-A-G

117202523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100741520-G-A

117202717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100741315-T-C

117202749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100741283-A-G

117202789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100741245-G-A

117202965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100741102-T-A

117202972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100741095-C-T

117203028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100741047-G-C

117203034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100741041-G-A

117203149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740927-C-T

117203325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740751-T-A

117203325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740751-T-C

117203468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740603-A-G

117203514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740563-G-C

117203514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740563-G-T

117203533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740544-T-C

117203590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740493-A-T

117203591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740492-G-T

117203603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740480-G-T

117203604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740479-C-G

117203604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740479-C-T

117203619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100740464-T-C

117203657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100740331-A-T

http://identifiers.org/hco/1/GRCh38#117203803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100740173-C-A

117203803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100740173-C-T

117203835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100740142-A-G

117203876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740112-G-A

117203876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740112-G-T

117203877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740111-G-A

117203877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740111-G-T

http://identifiers.org/hco/1/GRCh38#117203906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100740082-C-A

117203906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740082-C-T

117203928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740068-T-A

117203928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740068-T-C

117203929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740067-T-C

117203931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740065-G-A

117203931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740065-G-T

117203976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740026-G-A

117203976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740026-G-T

117203977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740025-G-C

117203977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740025-G-T

117204021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100739980-C-T

117204059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100739937-A-G

117204336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100739689-G-A

117205752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100738655-C-T

117205967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100737979-T-C

117205991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100737964-C-T

http://identifiers.org/hco/1/GRCh38#117206016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100737939-C-A

117207334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100736024-T-C

http://identifiers.org/hco/1/GRCh38#117207649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#100735760-C-A

117207667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100735742-G-A

117207679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100735730-G-A

117208622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100734951-C-T

117208929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100734709-T-C

117208973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100734665-T-C

117209389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100734274-A-G

117209459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100734205-C-T

117209512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100734175-G-A

117209604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100734093-A-G

117209629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100734068-T-C

117209895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100733852-T-C

117210001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100733751-T-C

117210315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100733357-G-A

117210315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100733357-G-T

http://identifiers.org/hco/1/GRCh38#117210693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#100733061-C-A

117210693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100733061-C-T

117210723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100733032-A-G

117210723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100733032-A-T

117210731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100733024-T-A

117210791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100732962-A-G

117210927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28873
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 100732773-C-G