http://identifiers.org/hco/17/GRCh38#143746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75659966-C-A

143961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75660174-C-G

http://identifiers.org/hco/17/GRCh38#144046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75660274-C-A

144046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75660274-C-T

144065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75660294-C-T

144217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75660453-G-C

http://identifiers.org/hco/17/GRCh38#144241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75660477-C-A

144241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75660477-C-T

144323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75660491-A-G

145060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75660890-G-T

145091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75660923-C-T

http://identifiers.org/hco/17/GRCh38#145137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75660974-C-A

145165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661001-G-C

145294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661098-A-G

http://identifiers.org/hco/17/GRCh38#145368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75661156-C-A

145368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661156-C-T

145413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661200-T-C

145515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661298-A-G

145557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661341-A-G

145566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661349-G-A

145566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661349-G-T

145567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661350-G-A

145567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661350-G-T

145621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661400-G-A

145621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661400-G-T

145636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661415-C-T

145642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661421-A-G

145948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661526-T-C

146250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661761-G-A

146250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661761-G-T

146285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661794-G-A

146285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661794-G-T

146320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661830-T-C

http://identifiers.org/hco/17/GRCh38#146351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75661863-C-A

146362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661874-G-A

146362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661874-G-T

146367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661879-G-A

146367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661879-G-T

http://identifiers.org/hco/17/GRCh38#146507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75661986-C-A

146507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75661986-C-T

146554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75662024-T-C

146584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75662053-C-T

146637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75662098-A-G

http://identifiers.org/hco/17/GRCh38#146671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75662137-C-A

146694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75662159-C-T

146817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75662285-T-C

146868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75662312-G-A

http://identifiers.org/hco/17/GRCh38#147060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75662402-C-A

147060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75662402-C-T

http://identifiers.org/hco/17/GRCh38#147070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75662410-C-A

147070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75662410-C-T

147074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75662414-G-A

147074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75662414-G-T

147177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75662517-G-T

147332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75662668-C-G

147332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75662668-C-T

147369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75662686-G-T

147516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75662833-C-T

147518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75662835-G-T

147555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75662872-G-A

147555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75662872-G-T

147608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75662928-A-G

147615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75662934-C-T

http://identifiers.org/hco/17/GRCh38#147622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75662941-C-A

147622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75662941-C-T

147623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75662942-T-C

http://identifiers.org/hco/17/GRCh38#147639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75662951-C-A

147695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75662952-T-C

147764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75663023-C-G

147928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75663182-C-T

148045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75663270-T-C

148045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75663270-T-G

148069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75663296-G-T

148164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75663340-C-G

148164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75663340-C-T

148289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75663465-G-A

148289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75663465-G-T

148704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75663894-G-C

148844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75664069-C-T

148974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75664220-T-A

148974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75664220-T-C

http://identifiers.org/hco/17/GRCh38#148989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75664234-C-A

148989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75664234-C-G

148989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75664234-C-T

149013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75664256-C-G

149013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75664256-C-T

149034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75664280-T-A

149034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75664280-T-C

149050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75664296-A-G

http://identifiers.org/hco/17/GRCh38#149102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75664353-C-A

149102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75664353-C-G

149102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75664353-C-T

149244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75664495-T-C

150299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75665199-G-A

150299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75665199-G-C

150945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75665981-G-A

155875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75667328-G-A

155875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75667328-G-C

155875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75667328-G-T

http://identifiers.org/hco/17/GRCh38#155884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75667334-C-A

155884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75667334-C-G

155884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75667334-C-T

155900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75667350-T-A

155900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75667350-T-C

155900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75667350-T-G

155938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75667444-C-T

http://identifiers.org/hco/17/GRCh38#155948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75667454-A-C

155948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75667454-A-G

155965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75667482-G-T

http://identifiers.org/hco/17/GRCh38#155985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75667544-C-A

155985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75667544-C-T

156040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75667633-T-A

156040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75667633-T-C

http://identifiers.org/hco/17/GRCh38#156049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75667642-C-A

156049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75667642-C-T

156067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75667659-T-C

156097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75667689-A-G

156129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75667732-T-C

156203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75667802-G-A

156203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75667802-G-C

156203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75667802-G-T

156205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75667804-G-A

156205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75667804-G-T

156354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75667960-G-A

156354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75667960-G-T

156393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75667999-G-T

http://identifiers.org/hco/17/GRCh38#156412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75668021-C-A

156412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75668021-C-G

156412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75668021-C-T

156429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75668052-G-T

156439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75668062-G-A

156439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75668062-G-T

156454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75668077-G-T

158338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75668098-T-C

http://identifiers.org/hco/17/GRCh38#158615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75668353-C-A

158615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75668353-C-G

159141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

160278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75668850-G-A

160325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75668881-G-T

160352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75668908-G-A

160665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75669161-C-T

160690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75669185-C-G

160690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant, stop_retained_variant
orthologous variants: 75669185-C-T

http://identifiers.org/hco/17/GRCh38#160771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75669270-C-A

160771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75669270-C-T

160875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75669374-A-G

http://identifiers.org/hco/17/GRCh38#161326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75670719-C-A

161326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75670719-C-G

161326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75670719-C-T

161360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75670772-C-G

161360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75670772-C-T

161368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75670780-C-T

161377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75670789-A-G

161445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75670895-G-A

161451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75670901-G-T

http://identifiers.org/hco/17/GRCh38#161552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75670999-C-A

161552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75670999-C-T

162137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75671137-G-A

162149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75671149-G-A

162164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75671164-G-A

http://identifiers.org/hco/17/GRCh38#162308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75671295-A-C

162586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75671493-A-G

162667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75671579-A-G

http://identifiers.org/hco/17/GRCh38#162762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75671673-C-A

162790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75671715-T-C

162790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75671715-T-G

164109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75672425-G-A

164109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75672425-G-T

http://identifiers.org/hco/17/GRCh38#164210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75672527-C-A

164210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75672527-C-G

164210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75672527-C-T

164311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75672605-G-A

164311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75672605-G-T

164577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75672814-G-A

164626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75672866-G-A

http://identifiers.org/hco/17/GRCh38#164690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75672929-A-C

164707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75672945-G-A

http://identifiers.org/hco/17/GRCh38#164773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75673013-A-C

164918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75673150-G-A

165218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75673470-A-G

165262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75673506-G-A

165390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75673564-G-A

http://identifiers.org/hco/17/GRCh38#165505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75673662-A-C

165506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75673663-A-G

165514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75673671-G-A

165515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75673672-G-T

165599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75673744-C-G

165630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75673773-C-T

http://identifiers.org/hco/17/GRCh38#165756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75673877-C-A

165799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75673906-G-C

165815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75673921-G-T

165848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75673954-C-T

166016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75674101-C-T

166017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75674102-G-A

166050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75674134-G-A

166422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75674482-G-C

169758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75675559-C-G

169971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75675747-C-G

169971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75675747-C-T

170045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75675815-T-C

170049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75675819-G-A

http://identifiers.org/hco/17/GRCh38#170081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75675849-C-A

170114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75675870-G-A

170192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75675955-G-C

170234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75675986-C-T

170235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75675987-G-A

170296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75676021-G-T

170348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75676073-T-A

170466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75676174-C-G

170501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75676217-T-G

170522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75676239-G-A

170612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75676324-T-C

170620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75676332-C-G

170620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75676332-C-T

172039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75676508-C-G

172107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75676572-C-T

172243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75676723-T-A

172420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75676833-G-A

172420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75676833-G-T

172500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75676894-G-A

172500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75676894-G-C

172500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75676894-G-T

172754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75678842-T-C

172755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75678843-A-G

http://identifiers.org/hco/17/GRCh38#172762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75678850-C-A

172762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75678850-C-T

172906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75678996-G-A

172906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75678996-G-T

172930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75679030-C-T

172965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75679077-C-T

173131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75679249-C-G

174047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75679799-C-T

174066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75679814-C-T

174199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75679915-G-A

174223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75679939-G-C

174483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75680132-T-C

http://identifiers.org/hco/17/GRCh38#174782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75680300-C-A

175656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75680979-T-C

175756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75681079-G-C

175964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75681182-G-T

176039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75681265-G-A

176180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75681418-G-A

176199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75681431-G-T

176212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75681444-G-T

176328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75681559-G-A

176343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75681571-C-T

176350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75681578-C-T

http://identifiers.org/hco/17/GRCh38#176714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75682172-A-C

177063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75682530-G-C

177063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75682530-G-T

177078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75682724-A-T

177179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75682842-T-C

177359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75683050-C-T

177360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75683051-A-G

177407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75683095-T-C

177694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75683309-G-A

177815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75683407-C-T

177848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75683436-C-T

177907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75683506-G-A

179466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75684876-G-C

179466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75684876-G-T

179586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75684997-G-A

179855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75685249-G-A

179921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75685305-T-A

179921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75685305-T-C

180141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75685555-C-T

http://identifiers.org/hco/17/GRCh38#180160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75685570-C-A

180160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75685570-C-T

180166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75685576-C-G

180218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75685624-C-T

180242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75685661-G-A

180242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75685661-G-T

180422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75685825-G-C

180456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75685858-G-A

180456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75685858-G-C

180677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75686031-C-G

180705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75686070-G-A

180738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75686103-C-T

http://identifiers.org/hco/17/GRCh38#181186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75686426-C-A

181186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75686426-C-G

181186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75686426-C-T

181194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75686434-G-A

181207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75686447-G-A

181207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75686447-G-T

http://identifiers.org/hco/17/GRCh38#181326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75686566-C-A

181326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75686566-C-G

181326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75686566-C-T

181360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75686600-G-A

181360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75686600-G-T

181513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75686751-G-A

181513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75686751-G-T

http://identifiers.org/hco/17/GRCh38#181515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75686753-C-A

181515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75686753-C-T

http://identifiers.org/hco/17/GRCh38#181531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75686769-C-A

181531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2986
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75686769-C-T