93040479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -T-C

93040501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -G-T

93040512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -T-A

93040512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -T-G

93040514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -A-G

93040514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -A-T

93040593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -T-C

93040626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -T-C

http://identifiers.org/hco/15/GRCh38#93040648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-A

http://identifiers.org/hco/15/GRCh38#93040689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-A

93040689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-T

93040774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -A-G

93040821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -G-A

93040842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -G-T

http://identifiers.org/hco/15/GRCh38#93041060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-A

93041060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-G

93041106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -G-A

93041106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -G-C

93041106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -G-T

http://identifiers.org/hco/15/GRCh38#93041157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-A

93041157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-T

http://identifiers.org/hco/15/GRCh38#93041192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-A

93041192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-T

http://identifiers.org/hco/15/GRCh38#93041213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-A

93041275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -G-T

http://identifiers.org/hco/15/GRCh38#93041292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-A

93041292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-T

93041307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -G-A

93041312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -T-C

http://identifiers.org/hco/15/GRCh38#93041336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-A

93041345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -G-A

http://identifiers.org/hco/15/GRCh38#93041370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-A

93041417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -T-C

93041435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -T-C

93041452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -G-A

93041452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -G-C

93041452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -G-T

http://identifiers.org/hco/15/GRCh38#93041466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-A

93041466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-T

93041601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -G-A

93041601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -G-T

http://identifiers.org/hco/15/GRCh38#93041678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-A

http://identifiers.org/hco/15/GRCh38#93041694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: -C-A

93041694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: -C-T

http://identifiers.org/hco/15/GRCh38#93041695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: -C-A

http://identifiers.org/hco/15/GRCh38#93041715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -C-A

93041860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: -T-C

93042570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73070313-T-C

93042592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73070292-T-C

93042633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73070254-T-A

93042633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73070254-T-C

http://identifiers.org/hco/15/GRCh38#93042637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73070250-C-A

93042672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73070213-A-T

93042689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73070195-A-G

93042735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73070147-T-C

93042735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73070147-T-G

http://identifiers.org/hco/15/GRCh38#93042763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73070131-C-A

93042763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73070131-C-T

93042791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73070103-G-T

93042803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73070091-G-A

93042863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73070035-G-A

93042863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73070035-G-C

93042863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73070035-G-T

http://identifiers.org/hco/15/GRCh38#93042873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73070025-C-A

93042873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73070025-C-T

93042882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73070022-C-T

93042884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73070020-G-A

http://identifiers.org/hco/15/GRCh38#93042927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73069980-C-A

93042927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73069980-C-G

93042963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73069939-G-A

93043036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73069877-A-G

93043045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73069868-T-C

93043089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73069820-T-C

93043157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3 prime UTR variant
orthologous variants: 73069770-C-T

http://identifiers.org/hco/15/GRCh38#93043475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73069574-C-A

93043475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069574-C-T

93043626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069420-G-T

93043664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069394-G-A

93043664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069394-G-C

93043714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069352-T-C

93043714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069352-T-G

93043759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069313-A-G

93043835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069253-A-G

93043839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069249-T-A

93043839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069249-T-C

93043839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069249-T-G

93043860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069236-G-T

93043932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069147-G-A

93043991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069090-G-A

93043991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069090-G-T

93044003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069078-C-T

93044015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069066-G-A

93044015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069066-G-T

http://identifiers.org/hco/15/GRCh38#93044032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73069047-C-A

93044032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069047-C-G

93044036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73069041-G-T

http://identifiers.org/hco/15/GRCh38#93044038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73069039-C-A

93044150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068899-T-C

93044165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068883-G-T

http://identifiers.org/hco/15/GRCh38#93044183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73068864-C-A

93044207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068830-G-A

93044222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068796-G-A

93044222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068796-G-C

93044222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068796-G-T

http://identifiers.org/hco/15/GRCh38#93044257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73068760-C-A

93044264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068752-T-C

93044372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068578-T-G

http://identifiers.org/hco/15/GRCh38#93044425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73068520-C-A

93044425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068520-C-G

93044425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068520-C-T

93044575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068333-T-A

93044575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068333-T-C

http://identifiers.org/hco/15/GRCh38#93044595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73068310-A-C

93044595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068310-A-G

93044595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068310-A-T

93044697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068209-G-A

93044697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068209-G-C

93044697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068209-G-T

93044703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068203-G-A

93044703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068203-G-T

93044747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068148-G-C

93044747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73068148-G-T

93044768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 73068127-T-A

93044768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 73068127-T-C

http://identifiers.org/hco/15/GRCh38#93044810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73068084-C-A

93044810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 73068084-C-T

http://identifiers.org/hco/15/GRCh38#93044831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73068063-A-C

93044831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 73068063-A-G

93044831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 73068063-A-T

93044851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 73067986-T-A

93044851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 73067986-T-G

93044867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 73067970-A-G

93044867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 73067970-A-T

93044882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 73067949-G-A

93044882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 73067949-G-C

93044882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 73067949-G-T

93044885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 73067946-T-C

93044885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 73067946-T-G

93044889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 73067942-G-A

93044889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 73067942-G-T

93045350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73067418-G-C

http://identifiers.org/hco/15/GRCh38#93045644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73067124-A-C

93045644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73067124-A-G

93045799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73066988-G-A

93045799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73066988-G-T

93045833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73066955-C-T

93045834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73066954-T-C

http://identifiers.org/hco/15/GRCh38#93045835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73066953-C-A

93045835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73066953-C-T

93045869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73066917-G-A

93045869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73066917-G-C

93045937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73066863-T-C

93046268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73066574-T-G

93046350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73066495-G-A

93048517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73064543-G-A

93048705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73064392-G-A

93048705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73064392-G-T

93048706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73064391-G-A

93048815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73064355-G-C

93048928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73064254-C-T

93048988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73064194-C-T

93049269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73063835-G-A

93049269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73063835-G-T

93049966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73063306-T-C

http://identifiers.org/hco/15/GRCh38#93050233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73063151-A-C

93050273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73063125-C-G

93050325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73063077-G-A

93050403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73062997-G-C

93050915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73062336-G-A

93050981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73062274-T-C

http://identifiers.org/hco/15/GRCh38#93050999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73062256-C-A

93051077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73062121-A-T

93051182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73062019-A-G

93051199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73062001-G-A

http://identifiers.org/hco/15/GRCh38#93051319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73061879-C-A

93051366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73061813-G-A

93051434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73061744-G-A

93051539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73061652-G-A

93051540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73061651-C-T

93051582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73061612-G-A

http://identifiers.org/hco/15/GRCh38#93051918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73061314-C-A

93051918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73061314-C-T

http://identifiers.org/hco/15/GRCh38#93052011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73059477-C-A

93052011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 73059477-C-T

93052405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73059083-G-A

93052405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73059083-G-T

93052456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73059029-G-A

93052456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73059029-G-T

93052489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73058996-A-G

93052880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73058046-G-A

93053319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

93053319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

93053362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

93053585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

93053616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

http://identifiers.org/hco/15/GRCh38#93053621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

93053621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/15/GRCh38#93056937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73055159-C-A

93056993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73055105-C-T

93057047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73055028-G-A

93057048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73055027-G-A

93057227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73054835-C-T

93057792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73054359-T-C

93057831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73054325-T-C

93057842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73054314-A-G

93057956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73054201-G-A

http://identifiers.org/hco/15/GRCh38#93057975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73054195-C-A

93058101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73054110-T-C

93058269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73053911-G-A

93059121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73053053-T-A

http://identifiers.org/hco/15/GRCh38#93059158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73053030-A-C

93059346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73052861-A-G

93059635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73052532-G-A

93059691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73052477-G-A

93059695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73052473-C-G

93059820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73052344-G-A

93059821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73052343-C-T

93060230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73051310-T-C

93060302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73051222-T-C

93061731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73050278-C-G

93061731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73050278-C-T

93061766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73050242-G-A

93061845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73050158-C-T

93061962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73050039-C-T

93062076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73049926-G-A

93062076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73049926-G-T

93062177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73049832-G-A

93062233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73049776-G-A

http://identifiers.org/hco/15/GRCh38#93062621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73049593-C-A

93062621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73049593-C-T

93062628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73049586-C-T

http://identifiers.org/hco/15/GRCh38#93062657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73049544-A-C

93062689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73049512-G-T

93062725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73049494-T-C

93062737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73049482-C-T

93062833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73049367-G-T

93062878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73049328-T-A

93062878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73049328-T-C

93062885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73049321-T-C

93062932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73049295-G-T

http://identifiers.org/hco/15/GRCh38#93062942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73049285-C-A

93062942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73049285-C-T

http://identifiers.org/hco/15/GRCh38#93062943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73049284-C-A

93063081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73049146-C-T

93063100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73049127-A-G

93063124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73049103-G-C

93063625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73048710-G-C

93063896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73048420-G-A

93063896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73048420-G-C

93063970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73048341-C-T

93064167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73048136-G-T

93064349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73047967-C-T

93066898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73047254-A-G

93067044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73047119-G-A

93067044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73047119-G-C

93067118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73047050-G-A

93067339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73046848-C-T

93067417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73046772-T-C

93067440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73046749-T-C

93067778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73046475-C-T

93067791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73046462-A-G

93067902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73046393-G-A

93067963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73046336-C-G

93068344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73046024-G-A

http://identifiers.org/hco/15/GRCh38#93068570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73045791-C-A

93068570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73045791-C-T

93068670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73045719-C-T

93068717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73045641-A-G

93068930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73045415-T-C

93068999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73045345-A-G

93069056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73045302-A-G

93069173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73045185-G-A

93069173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73045185-G-C

93069460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73045029-G-A

93069460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73045029-G-C

93069460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73045029-G-T

93069528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73044959-A-G

93069564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73044923-G-A

93069864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73044564-C-T

93069950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73044479-A-G

93070486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73043825-T-G

93071696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73042403-G-A

93071817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73042280-G-A

93072296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73041816-C-T

93072667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73041475-G-A

93072824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73041320-A-G

93072948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73041210-G-A

93072948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73041210-G-T

93073099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73041051-G-A

93073142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73041008-G-A

93073142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73041008-G-C

93073142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73041008-G-T

93073157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040993-G-A

93073157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040993-G-C

93073157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040993-G-T

http://identifiers.org/hco/15/GRCh38#93073162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73040987-C-A

93073167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040982-C-G

93073167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040982-C-T

http://identifiers.org/hco/15/GRCh38#93073178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73040971-C-A

93073178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040971-C-G

93073178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040971-C-T

93073191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040954-C-G

93073191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040954-C-T

93073194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040951-T-A

93073194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040951-T-C

93073194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040951-T-G

93073223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040922-T-A

93073223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040922-T-C

93073223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040922-T-G

93073225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040920-T-A

93073225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040920-T-C

93073225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040920-T-G

http://identifiers.org/hco/15/GRCh38#93073245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73040901-A-C

93073245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 73040901-A-G

93073272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 73040873-T-C

93073272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 73040873-T-G

http://identifiers.org/hco/15/GRCh38#93073280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73040865-C-A

93073280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040865-C-T

93073287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040858-G-A

93073287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040858-G-T

93073531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040648-A-G

93073533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73040646-A-T

93073562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: 73040622-A-G

http://identifiers.org/hco/15/GRCh38#93073600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73040583-C-A

93073600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73040583-C-G

93073600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73040583-C-T

http://identifiers.org/hco/15/GRCh38#93073733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73040458-C-A

93073733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 73040458-C-T

93073783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73040408-C-G

93073815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73040376-G-C

93073828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73040363-T-C

93073847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73040336-C-G

93073849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73040334-T-C

93073849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73040334-T-G

93074061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73040121-A-G

93074170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73040013-T-A

93074170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73040013-T-C

93074170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73040013-T-G

http://identifiers.org/hco/15/GRCh38#93074191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73039995-A-C

93074191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73039995-A-G

93074191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73039995-A-T

93074334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73039878-G-A

93074359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73039860-C-T

93074792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73039415-C-G

93074792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73039415-C-T

93074856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73039348-T-A

93078596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73037039-T-C

93078811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73036815-G-C

93078881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73036749-A-G

93079000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73036648-T-C

93079257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73036388-C-T

93079324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73036316-G-T

93079410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73036242-G-C

93080486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73034259-G-A

93080525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73034226-T-C

93080536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73034215-C-T

93080578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73034195-A-G

http://identifiers.org/hco/15/GRCh38#93080774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73034026-C-A

93080774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73034026-C-G

93080774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73034026-C-T

93080776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73034024-C-T

93080959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73033845-T-C

93080963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73033841-C-T

93081106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73033707-G-T

http://identifiers.org/hco/15/GRCh38#93081196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73033621-C-A

93081201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73033604-G-C

93081288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73033517-T-C

93081648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73032782-A-G

93081693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73032731-A-G

93081895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73032541-C-T

93081971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73032462-G-A

93081987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73032446-G-A

93082246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73032227-T-G

93082250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73032223-G-A

93082347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73032150-A-T

93082412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73032083-A-T

93082592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73031894-T-C

http://identifiers.org/hco/15/GRCh38#93082622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73031864-C-A

93082651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73031835-T-A

93082651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73031835-T-C

93082912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73031570-T-C

93082977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73031506-G-T

93082991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73031475-G-C

93083018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73031457-T-C

93083111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73031359-G-A

93083177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73031296-C-T

http://identifiers.org/hco/15/GRCh38#93083327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73031066-A-C

93083411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73030965-C-T

93083691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73030490-A-T

93083945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73030332-G-T

93084084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73030194-C-G

http://identifiers.org/hco/15/GRCh38#93084436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73029911-C-A

93084806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73029864-G-A

93084841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73029830-G-C

93085304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73029397-G-A

93085304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73029397-G-C

93086127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73028663-A-G

93086144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73028645-G-A

http://identifiers.org/hco/15/GRCh38#93086212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73028572-A-C

93086304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73028512-C-T

http://identifiers.org/hco/15/GRCh38#93086473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73028356-C-A

93086473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73028356-C-T

93086562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73028060-T-C

http://identifiers.org/hco/15/GRCh38#93086809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73027855-C-A

93087020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73027702-G-A

93087107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73027487-G-T

93087110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73027425-A-G

93087125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73027402-G-T

93087148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73027379-C-T

93087315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73027204-T-C

93087460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73027099-T-C

93087460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73027099-T-G

93087498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73027024-T-G

http://identifiers.org/hco/15/GRCh38#93087522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73027000-C-A

93087707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73026813-C-G

93087707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73026813-C-T

93087800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73026731-G-A

http://identifiers.org/hco/15/GRCh38#93087819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73026713-C-A

http://identifiers.org/hco/15/GRCh38#93087901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73026638-C-A

93087961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron_variant, undefined
orthologous variants: 73026577-T-C

93087961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron_variant, undefined
orthologous variants: 73026577-T-G

93088112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron_variant, undefined
orthologous variants: 73026426-T-C

93088112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron_variant, undefined
orthologous variants: 73026426-T-G

http://identifiers.org/hco/15/GRCh38#93088345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73026192-A-C

93088345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73026192-A-G

93088345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73026192-A-T

93088358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73026179-T-C

93088409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73026139-G-A

93088453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73026107-G-A

93088453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73026107-G-T

93088619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73025924-G-T

http://identifiers.org/hco/15/GRCh38#93088649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73025895-C-A

93088649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73025895-C-T

93088652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73025892-G-A

93088652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73025892-G-T

93088692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73025852-G-A

93088692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73025852-G-C

93088692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73025852-G-T

93088763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73025774-G-A

93088763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73025774-G-T

93088765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73025772-T-A

93088765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73025772-T-C

93088765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73025772-T-G

93088790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron_variant, undefined
orthologous variants: 73025747-T-A

93088790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron_variant, undefined
orthologous variants: 73025747-T-C

http://identifiers.org/hco/15/GRCh38#93088833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73025716-C-A

93088833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73025716-C-G

93088833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73025716-C-T

93088895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73025653-G-A

93088895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73025653-G-C

93088895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: intron variant
orthologous variants: 73025653-G-T

93089034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5 prime UTR variant
orthologous variants: 73025518-C-G

93089034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5 prime UTR variant
orthologous variants: 73025518-C-T

93089097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5 prime UTR variant
orthologous variants: 73025456-C-T

93089189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30308
most severe consequence: 5 prime UTR variant
orthologous variants: 73025360-C-T