485275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998118-T-G

http://identifiers.org/hco/6/GRCh38#485491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30998288-C-A

485526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998314-A-G

http://identifiers.org/hco/6/GRCh38#485626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30998385-C-A

485626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998385-C-T

485641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998398-G-A

http://identifiers.org/hco/6/GRCh38#485698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30998428-C-A

http://identifiers.org/hco/6/GRCh38#485754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30998485-C-A

http://identifiers.org/hco/6/GRCh38#485775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30998506-C-A

485780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998511-A-G

485831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998541-G-A

485831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998541-G-T

485905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998614-A-G

485956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998637-T-C

486004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998682-G-C

486029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998710-T-G

486086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998767-T-C

486136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998812-A-G

486159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998833-T-G

486188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998862-G-C

486188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998862-G-T

486223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998885-G-A

486223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998885-G-T

486278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30998928-T-C

486370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30999017-T-A

486448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30999071-A-G

486481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30999099-A-G

486512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30999131-T-A

486512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30999131-T-G

486524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30999152-T-C

http://identifiers.org/hco/6/GRCh38#486529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30999157-C-A

486529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30999157-C-T

486553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30999185-G-T

http://identifiers.org/hco/6/GRCh38#486609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30999229-C-A

486609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30999229-C-T

486625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30999245-T-C

486775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30999385-G-A

488124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31001278-C-T

http://identifiers.org/hco/6/GRCh38#488250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31001388-A-C

http://identifiers.org/hco/6/GRCh38#488407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31001520-A-C

488407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001520-A-T

488448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001563-G-C

488562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001654-A-T

http://identifiers.org/hco/6/GRCh38#488578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31001669-C-A

488601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001701-G-A

488949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001950-T-C

489484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31002502-G-A

http://identifiers.org/hco/6/GRCh38#489543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31002584-C-A

489727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31002762-T-C

489973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31003022-C-T

490318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31003755-T-A

490318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31003755-T-G

490365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31003817-T-A

490365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31003817-T-C

490393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31003845-G-A

490414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31003869-G-A

490508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31003950-T-A

490520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31003963-A-G

490587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31004013-C-T

491157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31004593-G-A

491163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31004599-C-G

491163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31004599-C-T

491230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004653-T-A

491260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004683-G-A

491260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004683-G-C

491316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004722-G-A

491316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004722-G-T

491364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004751-A-G

491829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31005116-G-A

497358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006606-T-C

497530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006787-T-C

497543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006800-G-A

497543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006800-G-C

http://identifiers.org/hco/6/GRCh38#497564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31006820-C-A

498055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31008754-T-C

498085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31008785-T-C

498085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31008785-T-G

498307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009038-T-C

498346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009075-A-T

http://identifiers.org/hco/6/GRCh38#498584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31009272-A-C

498584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009272-A-G

498953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009514-C-T

499911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31010275-G-T

499925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31010289-T-C

499959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31010318-C-T

500297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31011016-G-C

500452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31011151-A-G

500552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31011242-G-A

500562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31011251-T-A

500562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31011251-T-C

500596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31011286-G-C

500620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31011305-A-T

500709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31011393-C-T

501981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31011736-C-T

501986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31011741-C-T

502013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31011757-T-G

502121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31011877-G-C

502183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31011946-G-T

http://identifiers.org/hco/6/GRCh38#502333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31012052-A-C

502467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012141-C-G

502493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012161-C-T

502584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012237-A-G

http://identifiers.org/hco/6/GRCh38#502670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31012325-A-C

503177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012807-T-A

503285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012911-T-C

503285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012911-T-G

503334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012953-C-T

503360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012976-C-T

503496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013066-T-C

504223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013623-G-A

504316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013738-C-T

504319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013748-G-A

504558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013997-G-A

http://identifiers.org/hco/6/GRCh38#504679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31014117-C-A

504692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014130-A-G

504692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014130-A-T

504852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014273-C-T

506262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015152-A-G

506403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015279-G-T

506414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015290-G-A

506684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015571-T-C

506955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015843-G-A

507451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015965-T-C

507574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016085-T-C

507586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016099-A-G

http://identifiers.org/hco/6/GRCh38#507593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31016106-A-C

507781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016268-A-G

507839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016321-T-C

507974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31016481-T-C

508081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31016613-C-G

508081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31016613-C-T

508326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31016876-T-C

508333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31016883-T-G

http://identifiers.org/hco/6/GRCh38#508452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31016998-C-A

509451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31017332-G-A

509451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31017332-G-T

509511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31017367-G-C

509706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31017532-C-T

510451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31018236-T-C

http://identifiers.org/hco/6/GRCh38#510691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31018480-C-A

510705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31018494-C-T

510739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31018535-T-C

511331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31019332-G-A

511337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31019342-C-G

511424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31019410-G-C

511543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31019523-G-A

511589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31019565-G-C

513289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31021149-A-G

513305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31021166-C-T

http://identifiers.org/hco/6/GRCh38#513399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31021278-A-C

513586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31021453-A-G

514371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31022343-T-C

514380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31022352-C-T

514399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31022360-T-C

515181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31024305-T-C

515310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31024426-C-T

515432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31024528-A-G

515489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31024665-C-T

515532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31024705-G-A

515814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025049-G-A

516026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025313-G-C

516148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025417-A-G

516260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025530-T-C

516295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025565-G-T

516439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025684-C-G

516439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025684-C-T

516513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025731-C-G

516513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025731-C-T

516564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025773-G-A

516756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025947-T-G

516778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025974-T-G

516978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31026175-G-T

517343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31026527-A-T

517360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31026544-A-G

517395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31026576-T-A

517419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31026597-A-G

517439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31026615-T-C

517516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31026690-T-C

517724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029359-C-T

518054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029719-A-G

518159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029823-A-T

518282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029942-C-T

518356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030012-T-C

518469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030116-T-A

518677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030316-C-T

518698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030337-A-G

521854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030927-A-G

521950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31031023-G-C

521975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31031047-C-T

522024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31031094-A-G

522168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31031242-G-T

527280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033198-G-A

527329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033250-C-T

527565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033474-C-T

527835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033743-T-C

528268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31034169-C-G

528711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31034545-C-T

http://identifiers.org/hco/6/GRCh38#528773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31034596-C-A

528774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31034597-A-G

http://identifiers.org/hco/6/GRCh38#529088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31034772-C-A

529287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31034960-G-A

529451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31035117-C-T

529452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31035118-G-A

532455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040621-A-T

532596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31040764-T-C

532596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31040764-T-G

http://identifiers.org/hco/6/GRCh38#532714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31040870-C-A

532714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040870-C-T

544738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045624-C-T

544786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045670-A-G

544816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045698-T-C

http://identifiers.org/hco/6/GRCh38#545183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31045739-A-C

545183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045739-A-G

545550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31046097-C-T

547732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31047379-C-T

547752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31047406-T-C

http://identifiers.org/hco/6/GRCh38#547860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31047512-C-A

548006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31047658-A-G

548006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31047658-A-T

548266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31047903-C-T

548741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048427-G-C

548760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048445-C-T

548817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048502-G-A

548892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048571-C-T

549059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048726-T-A

549059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048726-T-C

549062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048729-G-A

549062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048729-G-T

549199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31048838-G-A

549199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31048838-G-C

549271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31048910-G-A

549315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048954-A-G

549343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048988-T-C

549343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048988-T-G

549917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049432-G-C

549959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049474-T-A

549959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049474-T-C

550069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049594-T-C

550180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049705-T-C

550292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049831-C-T

550499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31050172-C-G

550503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31050177-G-A

550629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31050313-G-A

550629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31050313-G-C

551004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31050653-T-C

551024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31050673-A-G

http://identifiers.org/hco/6/GRCh38#553439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31051640-A-C

553439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051640-A-G

553507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051682-A-G

http://identifiers.org/hco/6/GRCh38#553959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31052063-C-A

555408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31055271-G-A

555408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31055271-G-T

555425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31055300-A-G

555425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31055300-A-T

555431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31055316-G-A

555687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31055606-G-A

555911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31055788-A-G

556042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31055920-T-C

556042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31055920-T-G

556074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31055955-G-A

http://identifiers.org/hco/6/GRCh38#556337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31056143-A-C

556603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31056390-G-A

559801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31057094-G-C

560370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31057610-A-G

http://identifiers.org/hco/6/GRCh38#560371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31057611-C-A

560393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31057632-T-C

560420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31057657-T-C

560420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31057657-T-G

562065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31058601-C-T

562066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31058602-C-G

562330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31058835-C-T

562410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31058887-G-A

562538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059008-C-G

562634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059090-G-T

http://identifiers.org/hco/6/GRCh38#562657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31059113-A-C

562657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059113-A-G

http://identifiers.org/hco/6/GRCh38#562659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31059115-C-A

http://identifiers.org/hco/6/GRCh38#562669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31059125-C-A

562669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059125-C-T

562685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059147-G-A

http://identifiers.org/hco/6/GRCh38#562696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31059162-C-A

562696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059162-C-T

562736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059194-T-A

562736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059194-T-C

562969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059419-A-G

562998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059448-T-C

563186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059595-T-A

563290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059680-C-T

563311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059698-C-G

563316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059703-T-A

563320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059707-G-A

563320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059707-G-T

563607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060321-A-T

563712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060409-C-T

http://identifiers.org/hco/6/GRCh38#563927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31060626-C-A

563935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060634-G-A

563935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060634-G-T

http://identifiers.org/hco/6/GRCh38#563945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31060644-C-A

563945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060644-C-G

563945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060644-C-T

563957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060656-G-T

563973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060672-G-A

564097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31060778-G-C

564193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060870-G-T

http://identifiers.org/hco/6/GRCh38#564197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31060875-C-A

564197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060875-C-G

564197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060875-C-T

564244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060920-G-A

564261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060937-G-A

564261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060937-G-T

564291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060948-A-G

564291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060948-A-T

564295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060952-G-C

564296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060953-G-A

564296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060953-G-C

564296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060953-G-T

564332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060976-G-A

564406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31061046-T-A

564406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31061046-T-G

564440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31061077-A-G

http://identifiers.org/hco/6/GRCh38#564484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31061141-C-A

564484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31061141-C-T

564676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31061357-G-A

564742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31061417-A-G

564800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31061481-A-G

564840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31061509-T-A

564958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31061625-A-G

565137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31061774-C-T

565187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31061822-G-A

565187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31061822-G-T

565841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31062520-T-C

565978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31062622-G-A

566211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31062784-G-T

566336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31062861-A-G

566765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31063133-C-T

566781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31063146-C-T

567162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31063508-T-C

567185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31063523-G-C

567376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31063661-A-G

567377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31063662-G-C

567430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31063709-C-T

569085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31064303-A-G

569124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31064340-T-A

569566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31064705-C-T

572510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31066222-G-A

573918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31067362-T-C

574138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31067514-A-G

574172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31067548-T-C

576725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070140-A-G

576803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31070218-T-C

576803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31070218-T-G

http://identifiers.org/hco/6/GRCh38#577019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31070397-A-C

578047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070962-C-T

578087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31071001-G-A

http://identifiers.org/hco/6/GRCh38#578229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31071133-A-C

578359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31071240-A-G

578797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31071955-G-A

http://identifiers.org/hco/6/GRCh38#578888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31072054-C-A

579080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31072234-C-T

579269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31072434-C-T

http://identifiers.org/hco/6/GRCh38#579426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#31072572-C-A

579426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31072572-C-T

579505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31072653-C-T

579798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31073121-C-G

579934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31073275-A-G

579952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31073292-T-C

580462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31073817-T-C

580680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31074045-G-A

580684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31074049-C-T

580953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31074270-T-C

582049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31074836-C-T

582168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075002-T-A

582313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075164-C-T

http://identifiers.org/hco/6/GRCh38#582456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31075304-A-C

582489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075337-G-A

582526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075374-T-C

582757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075562-A-G

582762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075567-T-C

582819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075617-T-C

582999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075790-G-T

583160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075892-T-C

583185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075919-T-C

http://identifiers.org/hco/6/GRCh38#583283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31076018-A-C

583283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076018-A-G

583426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076159-G-A

http://identifiers.org/hco/6/GRCh38#584028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31077532-C-A

584451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31077905-G-A

http://identifiers.org/hco/6/GRCh38#584721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31078220-C-A

584809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31078307-C-T

584851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31078335-T-C

584887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31078374-A-G

585350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31078872-C-T

585792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079053-G-A

585793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079054-T-C

586010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079279-C-T

586094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079369-C-T

586104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079379-T-C

586448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079675-T-C

586448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079675-T-G

586775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079965-G-A

586861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31080003-G-A

587049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31080131-T-C

588359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31081404-T-A

588505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31081524-C-T

588889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31081811-C-T

588906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31081851-T-A

http://identifiers.org/hco/6/GRCh38#588950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31081907-C-A

589165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31082077-G-A

590407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31082873-G-A

590454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31082918-G-C

http://identifiers.org/hco/6/GRCh38#590534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31082997-C-A

http://identifiers.org/hco/6/GRCh38#590611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31083062-C-A

http://identifiers.org/hco/6/GRCh38#590778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31083245-C-A

590798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31083265-G-C

590942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31083428-C-T

591034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31083504-G-A

591100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31083539-T-A

http://identifiers.org/hco/6/GRCh38#591427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31083781-C-A

591745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31084031-C-T

591786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31084063-A-G

592062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31084337-T-A

http://identifiers.org/hco/6/GRCh38#592112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31084404-A-C

http://identifiers.org/hco/6/GRCh38#592264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31084563-C-A

592264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31084563-C-T

592321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31084655-T-A

http://identifiers.org/hco/6/GRCh38#592333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31084667-C-A

592435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31084737-G-A

592435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31084737-G-C

592435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31084737-G-T

592450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31084749-T-C

592500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31084799-A-G

592518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31084817-G-A

592697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31084963-A-G

593776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31086253-C-G

593895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31086361-A-T

594078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31086546-T-A

594078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31086546-T-C

594079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31086547-G-A

594158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31086632-A-G

594370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31086848-G-A

594382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31086860-C-T

594490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31086953-G-C

594502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31086965-G-C

594812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31087245-A-T

594861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31087293-T-C

594895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31087327-G-A

595148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31087617-T-C

596962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31088921-G-A

597103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31089058-C-G

597933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31089556-G-T

597972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31089588-G-A

597972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31089588-G-T

598008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31089623-G-T

598135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31089750-G-A

598135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31089750-G-T

598191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31089798-G-T

598213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31089814-G-T

598414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31090015-A-G

598455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31090092-G-T

598538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31090175-G-C

598739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31090364-T-G

598817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31090444-T-C

599032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31090675-A-G

599038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31090681-G-T

http://identifiers.org/hco/6/GRCh38#599049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31090692-C-A

599075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31090710-T-A

599075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31090710-T-G

599755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31091293-T-C

599815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31091351-T-A

599892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31091422-G-T

599914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31091443-G-A

600423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31091936-C-T

600434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31091947-T-C

600454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31091971-T-C

http://identifiers.org/hco/6/GRCh38#600819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31092306-C-A

601169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31092618-G-A

602575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31092758-C-T

602613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31092806-T-C

http://identifiers.org/hco/6/GRCh38#602656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31092826-C-A

602739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31092914-G-A

602753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31092936-T-C

602754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31092937-G-T

602776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31092965-T-A

603194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31093322-C-T

603582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31093689-C-G

603638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31093736-G-T

608944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31094160-G-A

608974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31094190-C-T

609758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31094920-C-T

609830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31094961-G-A

http://identifiers.org/hco/6/GRCh38#610273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31095337-C-A

610273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31095337-C-T

http://identifiers.org/hco/6/GRCh38#610313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31095377-C-A

611077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31096987-C-T

http://identifiers.org/hco/6/GRCh38#611328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31097133-C-A

612034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31097823-A-G

612103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31097916-C-G

http://identifiers.org/hco/6/GRCh38#612264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31098056-C-A

http://identifiers.org/hco/6/GRCh38#612377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31098175-A-C

612435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31098233-G-A

612482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31098538-T-C

http://identifiers.org/hco/6/GRCh38#613144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31099189-C-A

613279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31099234-T-C

613388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31099341-G-C

613937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31099831-T-C

613989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31099882-T-C

617159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31109141-T-C

617179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31109171-T-G

http://identifiers.org/hco/6/GRCh38#617193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31109179-A-C

617300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31109275-G-A

617427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31109425-G-A

617427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31109425-G-C

http://identifiers.org/hco/6/GRCh38#617591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#31109586-C-A

http://identifiers.org/hco/6/GRCh38#617645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#31109640-C-A

617645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31109640-C-T

http://identifiers.org/hco/6/GRCh38#617693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#31109688-C-A

617808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 31109803-G-A

617866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31109863-C-T

http://identifiers.org/hco/6/GRCh38#618253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31110183-C-A

http://identifiers.org/hco/6/GRCh38#619253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31111125-C-A

619360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31111220-G-T

619375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31111236-C-T

619569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31111429-T-C

619587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31111446-G-A

619587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31111446-G-C

619587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31111446-G-T

619688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31111530-G-A

619693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31111535-T-C

619693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31111535-T-G

http://identifiers.org/hco/6/GRCh38#619941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31111633-C-A

619985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31111676-T-C

620178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31111866-C-T

620240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31111914-C-T

620277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31111956-C-T

620334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31112034-C-G

http://identifiers.org/hco/6/GRCh38#620483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31112178-C-A

620483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31112178-C-T

620710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31112381-C-T

623768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31113965-G-A

624002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31114183-A-G

624916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31114432-T-G

624966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31114477-G-C

625003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31114511-G-A

625444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31114777-T-C

626163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31115455-C-T

626397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31115687-C-T

626499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31115782-G-A

628423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31117095-G-A

628482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31117138-A-G

628864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31118413-C-G

629000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31118537-C-G

629141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31118692-A-G

629715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31119373-T-G

http://identifiers.org/hco/6/GRCh38#629840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31119483-A-C

629906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31119549-G-T

629980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31119616-T-C

630461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31120045-C-T

630696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31120267-T-C

630859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31120409-C-G

631030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31120571-A-G

631117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31120669-G-A

631129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31120681-G-C

631988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31121282-G-C

632236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31121497-G-A

632435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31121648-C-T

632655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31121793-A-G

632726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31121834-T-A

http://identifiers.org/hco/6/GRCh38#632790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31121960-C-A

http://identifiers.org/hco/6/GRCh38#632802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31121982-C-A

632834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31122010-T-G

http://identifiers.org/hco/6/GRCh38#632862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31122039-C-A

632862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31122039-C-T

632865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31122043-A-G

633086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31122244-C-G

http://identifiers.org/hco/6/GRCh38#633149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31122305-C-A

633395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31122469-A-G

633449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31122507-T-C

633449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31122507-T-G

633637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31122696-T-C

633648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31122707-C-T

http://identifiers.org/hco/6/GRCh38#633799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31122862-A-C

http://identifiers.org/hco/6/GRCh38#634025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31123128-A-C

636646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31124150-G-C

636690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31124193-T-C

636785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31124265-C-T

637665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31124559-G-A

637665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31124559-G-T

637967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31124850-A-G

http://identifiers.org/hco/6/GRCh38#638003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31124889-C-A

638135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31124999-A-T

638162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31125026-T-A

http://identifiers.org/hco/6/GRCh38#641864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31125388-A-C

646921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31128941-T-G

647371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31129382-T-C

655790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130538-G-A

655790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130538-G-C

655790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130538-G-T

http://identifiers.org/hco/6/GRCh38#656000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31130714-C-A

656000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31130714-C-T

656014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31130727-T-C

656172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31130891-G-C

656172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31130891-G-T

656273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31130992-C-T

656393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31131112-G-A

656393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31131112-G-C

656404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31131123-C-G

656404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31131123-C-T

http://identifiers.org/hco/6/GRCh38#656418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31131137-C-A

656476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31131195-T-C

656498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31131217-G-C

656498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31131217-G-T

656546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31131265-G-A

656546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31131265-G-C

http://identifiers.org/hco/6/GRCh38#656674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31131393-C-A

656674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31131393-C-G

656674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31131393-C-T

http://identifiers.org/hco/6/GRCh38#656675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31131394-C-A

656675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31131394-C-T

http://identifiers.org/hco/6/GRCh38#656845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31131558-C-A

656845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31131558-C-G

656845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31131558-C-T

http://identifiers.org/hco/6/GRCh38#657021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31131802-C-A

657021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31131802-C-T

http://identifiers.org/hco/6/GRCh38#657081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31131852-C-A

657081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31131852-C-T

657136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31131887-G-A

657136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31131887-G-C

657136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31131887-G-T

657551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31132333-G-A

674364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31142224-T-G

674432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31142784-C-T

680139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31146493-C-G

680168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31146522-G-C

680289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31146641-G-A

680354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31146711-C-T

680362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31146719-C-T

680454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31146799-G-A

http://identifiers.org/hco/6/GRCh38#680499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31146843-C-A

680499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31146843-C-G

680513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31146857-T-C

680574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31146917-C-T

680635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31146964-G-C

680639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31146968-G-A

681048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31147180-T-C

681312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31147870-G-A

http://identifiers.org/hco/6/GRCh38#681538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31148179-A-C

681964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31148564-T-C

682059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31148649-C-T

682096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31148685-C-G

http://identifiers.org/hco/6/GRCh38#682552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31148803-C-A

682552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31148803-C-T

682944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149687-A-T

682981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149726-A-G

683274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149985-G-A

683336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150047-G-A

683837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150526-A-G

683893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150582-T-C

683933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150619-G-A

684269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150953-A-G

684271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150955-A-G

684275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150960-G-C

684332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31151008-G-A

684585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31151251-G-C

http://identifiers.org/hco/6/GRCh38#686590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31152359-C-A

686803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31152528-G-C

687072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31152717-G-C

687128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31152778-G-A

687128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31152778-G-C

687568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31152911-G-A

687815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31153094-T-C

688000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31153266-G-A

688154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31153399-G-A

688180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31153417-G-A

http://identifiers.org/hco/6/GRCh38#688945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31153838-C-A

688988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31153880-C-G

689334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31154167-T-G

689462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31154272-T-C

689462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31154272-T-G

689865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31154611-T-C

691886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31157451-T-C

691903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31157468-C-G

http://identifiers.org/hco/6/GRCh38#693041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31157987-C-A

693041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31157987-C-G

693041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31157987-C-T

693047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31157993-C-T

693053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31157996-A-G

693053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31157996-A-T

693057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31158000-A-G

693083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31158026-T-C

693090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31158033-C-T

http://identifiers.org/hco/6/GRCh38#693124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24968
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31158063-C-A