76461689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 5 prime UTR variant
orthologous variants: 136023672-C-G

http://identifiers.org/hco/7/GRCh38#76461754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136023738-A-C

76461869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136023853-T-C

76461892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136023877-G-A

76461892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136023877-G-C

76461892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136023877-G-T

76461985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136023968-G-A

76461985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136023968-G-C

76462228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136024168-C-T

76462256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136024215-G-T

76462805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136024518-C-G

76462831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136024543-C-T

76462918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136024624-T-C

76463033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136024717-C-G

76463392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136024997-T-A

76463392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136024997-T-C

76463462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136025070-C-T

76463719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136025316-A-G

76463720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136025317-T-C

76463737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136025335-T-C

76463797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136025693-A-G

http://identifiers.org/hco/7/GRCh38#76463856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136025752-A-C

76464054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136026681-G-A

76464155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136026781-G-A

76464155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136026781-G-C

76464155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136026781-G-T

76464239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136026867-A-G

76465436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136028519-G-A

76465451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136028534-T-A

76465451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136028534-T-G

http://identifiers.org/hco/7/GRCh38#76472199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136032038-C-A

76472199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136032038-C-T

76472238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136032084-A-G

76472341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136032227-G-T

76472356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136032239-G-T

76472395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136032285-C-T

76472405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136032295-C-T

76472409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136032299-C-G

76472409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136032299-C-T

76472480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136032372-C-G

76473251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136033780-C-G

76473373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136033896-C-T

76476186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136034366-A-G

http://identifiers.org/hco/7/GRCh38#76476199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136034379-A-C

76476402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136034577-T-A

76476402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136034577-T-C

76476587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136034934-G-C

http://identifiers.org/hco/7/GRCh38#76476622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136034968-C-A

76476698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136035035-A-G

http://identifiers.org/hco/7/GRCh38#76476879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136035183-C-A

http://identifiers.org/hco/7/GRCh38#76476880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136035184-C-A

76476931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136035216-T-A

76476931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136035216-T-C

76476931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136035216-T-G

http://identifiers.org/hco/7/GRCh38#76476953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136035235-C-A

76476953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136035235-C-T

76476969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136035251-G-T

http://identifiers.org/hco/7/GRCh38#76477143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136035412-C-A

76477195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136035451-A-G

76477217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136035473-G-A

76477312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136035558-G-A

http://identifiers.org/hco/7/GRCh38#76480331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136038800-A-C

76480331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136038800-A-G

76480398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136038851-G-T

76480590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136039023-G-A

76480590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136039023-G-C

76480590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136039023-G-T

http://identifiers.org/hco/7/GRCh38#76482509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136040866-C-A

76482509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 136040866-C-T

76482803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: synonymous variant
orthologous variants: 136041160-G-A

76482866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: synonymous variant
orthologous variants: 136041223-C-T

76483059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: synonymous variant
orthologous variants: 136041413-C-T

76483094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: synonymous variant
orthologous variants: 136041448-C-G

76483115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: synonymous variant
orthologous variants: 136041469-G-A

76483115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: synonymous variant
orthologous variants: 136041469-G-T

76483186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron variant
orthologous variants: 136041523-G-A

76483271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron variant
orthologous variants: 136041588-T-C

76485874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron variant
orthologous variants: 136044517-C-T

76486076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron variant
orthologous variants: 136044701-C-T

76486111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron variant
orthologous variants: 136044736-T-G

76486198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron variant
orthologous variants: 136044849-G-A

76486198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron variant
orthologous variants: 136044849-G-C

76486218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, undefined
orthologous variants: 136044924-T-A

76486321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, undefined
orthologous variants: 136045161-C-G

76486387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, undefined
orthologous variants: 136045230-C-T

76486394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, undefined
orthologous variants: 136045234-G-T

76486441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, undefined
orthologous variants: 136045291-T-G

76486499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, undefined
orthologous variants: 136045388-G-A

76486499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, undefined
orthologous variants: 136045388-G-T

http://identifiers.org/hco/7/GRCh38#76486661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#136045549-C-A

76488932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron variant
orthologous variants: 136048421-C-G

http://identifiers.org/hco/7/GRCh38#76489000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136048471-C-A

76489150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron variant
orthologous variants: 136048589-A-G

http://identifiers.org/hco/7/GRCh38#76492231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136050690-C-A

76492231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136050690-C-T

76492240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136050699-G-A

76492598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136050993-A-G

http://identifiers.org/hco/7/GRCh38#76496147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136053857-A-C

76496224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136053934-G-A

76496435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136054094-G-C

76496548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136054216-G-A

76496582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136054249-C-T

76496695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136054513-T-C

76496725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136054559-C-G

76496788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136054632-T-G

76496828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136054703-G-A

76496908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136054769-C-T

76497030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136054962-G-T

76497075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136055031-C-T

76497178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136055155-C-T

76497214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136055203-T-A

http://identifiers.org/hco/7/GRCh38#76497222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136055210-C-A

76497222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136055210-C-T

76497240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136055228-C-G

http://identifiers.org/hco/7/GRCh38#76497412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136055396-C-A

76497412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 136055396-C-G

76497412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 136055396-C-T

http://identifiers.org/hco/7/GRCh38#76497413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136055397-C-A

76497413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 136055397-C-T

http://identifiers.org/hco/7/GRCh38#76497561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136055528-C-A

76497561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136055528-C-T

http://identifiers.org/hco/7/GRCh38#76499879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136056855-A-C

76499931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136056926-G-C

76500057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 136057034-G-A

76500057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 136057034-G-T

76500072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057049-T-A

76500072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057049-T-C

76500072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057049-T-G

http://identifiers.org/hco/7/GRCh38#76500100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136057081-C-A

76500100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057081-C-G

76500249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057163-G-A

http://identifiers.org/hco/7/GRCh38#76500251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136057165-C-A

76500251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057165-C-G

76500251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057165-C-T

76500311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057210-G-A

76500314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057213-C-G

76500314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057213-C-T

76500353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057252-T-G

76500381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057278-T-A

76500381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057278-T-C

76500428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057340-T-A

76500428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057340-T-C

76500428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057340-T-G

76500493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136057399-G-A

76502217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_lost
orthologous variants: 136057835-T-C

http://identifiers.org/hco/7/GRCh38#76502232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136057850-C-A

76502232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057850-C-G

76502232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136057850-C-T

http://identifiers.org/hco/7/GRCh38#76502702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136058532-C-A

76502702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136058532-C-G

76502702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136058532-C-T

76503410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136059318-C-G

76503410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136059318-C-T

76503545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136059453-C-T

76503616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136059524-C-G

76503616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136059524-C-T

http://identifiers.org/hco/7/GRCh38#76503626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136059534-C-A

76503626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136059534-C-G

76503626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136059534-C-T

http://identifiers.org/hco/7/GRCh38#76503640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136059548-C-A

76503640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136059548-C-T

http://identifiers.org/hco/7/GRCh38#76503641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136059549-C-A

http://identifiers.org/hco/7/GRCh38#76503642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136059550-C-A

http://identifiers.org/hco/7/GRCh38#76503659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136059565-C-A

76503659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136059565-C-G

76503659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136059565-C-T

76503698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136059585-C-G

76503698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136059585-C-T

http://identifiers.org/hco/7/GRCh38#76503702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136059589-C-A

76503702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136059589-C-T

76503707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136059594-A-G

76503913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136059714-G-A

76503913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136059714-G-C

76503913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136059714-G-T

76503969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136059760-G-T

http://identifiers.org/hco/7/GRCh38#76504247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136059937-A-C

http://identifiers.org/hco/7/GRCh38#76504289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136059977-C-A

76504343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136060027-G-A

76504343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136060027-G-C

76504343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136060027-G-T

76504361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136060045-T-C

76504412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136060096-G-T

http://identifiers.org/hco/7/GRCh38#76504465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136060158-C-A

76504465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136060158-C-G

76504465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136060158-C-T

76504489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136060187-A-G

76504489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136060187-A-T

http://identifiers.org/hco/7/GRCh38#76504543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136060238-A-C

76504543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136060238-A-G

76504543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136060238-A-T

76505241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136060959-A-G

76505272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136060994-G-A

76505283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136061005-G-T

http://identifiers.org/hco/7/GRCh38#76505290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136061020-C-A

76505290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136061020-C-G

76505318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136061046-A-G

http://identifiers.org/hco/7/GRCh38#76505343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136061096-C-A

76505343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136061096-C-T

http://identifiers.org/hco/7/GRCh38#76505415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136061155-C-A

76505442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136061182-G-A

76505442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136061182-G-T

http://identifiers.org/hco/7/GRCh38#76505457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136061197-C-A

76505457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136061197-C-G

76505457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136061197-C-T

76505469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136061209-C-T

76505529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136061269-C-T

http://identifiers.org/hco/7/GRCh38#76505805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#136061554-C-A

76505805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136061554-C-T

76505910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136061649-C-T