1493377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 25334918-C-G

1493414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 25334883-G-T

1493563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 25334733-G-A

1494330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 25334195-C-T

1494332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 25334193-T-A

1494513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 25334012-C-T

http://identifiers.org/hco/16/GRCh38#1494518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#25334007-C-A

1494518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 25334007-C-T

1495310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25332267-G-A

http://identifiers.org/hco/16/GRCh38#1495327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25332250-A-C

http://identifiers.org/hco/16/GRCh38#1495329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25332248-C-A

1495329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25332248-C-G

1495329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25332248-C-T

1495414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 25332161-T-C

1495585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 25331990-T-C

1495590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 25331985-C-G

1495590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 25331985-C-T

1495596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 25331979-C-T

1495650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25331924-T-C

1495709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25331878-G-A

1495733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25331863-T-C

http://identifiers.org/hco/16/GRCh38#1495762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25331833-C-A

1495762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25331833-C-G

1495762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25331833-C-T

1495809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25331794-C-T

1495916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25331622-G-A

1495917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25331621-G-A

http://identifiers.org/hco/16/GRCh38#1496127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25331362-C-A

1496137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25331351-C-G

1496259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25331243-C-T

http://identifiers.org/hco/16/GRCh38#1496260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25331242-C-A

1496336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25331162-T-C

1496377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25331125-A-G

1496675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25330640-C-G

1496764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25330479-C-T

1496972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25330224-A-G

http://identifiers.org/hco/16/GRCh38#1496997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25330195-C-A

http://identifiers.org/hco/16/GRCh38#1497023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25330169-C-A

1497059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 25330133-T-G

1497117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25330075-G-C

1497117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25330075-G-T

http://identifiers.org/hco/16/GRCh38#1497129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25330065-C-A

1497129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25330065-C-G

1497132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25330062-T-C

http://identifiers.org/hco/16/GRCh38#1497219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25329979-C-A

1497219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329979-C-G

1497219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329979-C-T

1497231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329966-G-A

1497231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329966-G-T

1497261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329932-T-C

http://identifiers.org/hco/16/GRCh38#1497272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25329916-C-A

1497279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329904-A-G

1497279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329904-A-T

1497309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329874-A-G

1497490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 25329697-T-A

1497490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 25329697-T-C

1497516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 25329664-G-A

1497516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 25329664-G-T

1497525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329655-T-C

1497584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329623-T-G

1497599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329609-C-T

http://identifiers.org/hco/16/GRCh38#1497600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25329608-C-A

1497600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329608-C-T

1499041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329466-G-A

1499090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329418-G-A

1499133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329395-G-A

1499133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329395-G-T

1499134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329394-G-T

1499295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 25329237-A-G

1499299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 25329233-C-T

http://identifiers.org/hco/16/GRCh38#1499343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25329189-C-A

1499343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329189-C-T

1499348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25329185-G-A

http://identifiers.org/hco/16/GRCh38#1500023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25326461-C-A

1500023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25326461-C-T

1500046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25326438-G-A

1500046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25326438-G-T

1500054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25326409-G-A

1500054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25326409-G-T

http://identifiers.org/hco/16/GRCh38#1500180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25326283-C-A

1500180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25326283-C-T

1500214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25326249-G-A

1500214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25326249-G-T

1500241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25326222-G-A

1500241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25326222-G-T

1500247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25326214-G-A

1500271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25326191-C-G

1500271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25326191-C-T

1500296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25326163-G-T

http://identifiers.org/hco/16/GRCh38#1500309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25326141-C-A

1500309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25326141-C-T

http://identifiers.org/hco/16/GRCh38#1500320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25326130-C-A

1500320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25326130-C-T

1500368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 25326081-A-G

1500395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 25326054-C-T

1500522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25325924-G-A

1500522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25325924-G-T

1500548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25325895-G-A

http://identifiers.org/hco/16/GRCh38#1500780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25325663-C-A

1500780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25325663-C-T

http://identifiers.org/hco/16/GRCh38#1500783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25325660-C-A

1500976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25325483-A-T

1501043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25325401-C-G

1501094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25325354-G-C

1501145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25325296-C-T

1501256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25325184-C-T

http://identifiers.org/hco/16/GRCh38#1501262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25325178-A-C

http://identifiers.org/hco/16/GRCh38#1501303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25325149-C-A

1501423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 25325037-G-A

1501464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 25324996-C-T

http://identifiers.org/hco/16/GRCh38#1501475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25324985-C-A

1501475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 25324985-C-T

1501558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25324921-G-A

1501558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25324921-G-T

1501562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25324917-C-T

1501630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25324847-C-G

1501630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 25324847-C-T

http://identifiers.org/hco/16/GRCh38#1501689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25324786-A-C

1501730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25324745-G-A

1501730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25324745-G-T

1501745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25324730-C-G

1501745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25324730-C-T

1501856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25324566-G-A

1501856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25324566-G-C

http://identifiers.org/hco/16/GRCh38#1501862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25324560-C-A

1501862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25324560-C-G

1501862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25324560-C-T

1502190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25324282-G-A

1502191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25324281-C-G

http://identifiers.org/hco/16/GRCh38#1502239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25324229-C-A

1502239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25324229-C-T

1502240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25324228-G-A

1502240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25324228-G-C

http://identifiers.org/hco/16/GRCh38#1502266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25324193-C-A

1502338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25324122-G-T

http://identifiers.org/hco/16/GRCh38#1502363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25324097-C-A

1502363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25324097-C-T

http://identifiers.org/hco/16/GRCh38#1502388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25324072-C-A

1502388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25324072-C-T

http://identifiers.org/hco/16/GRCh38#1502474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25323970-C-A

1502474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25323970-C-T

1502501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25323950-G-A

1502501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25323950-G-T

1502599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25323939-G-T

1502617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25323921-G-T

1502696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25323845-G-A

1502696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25323845-G-T

1502778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25323764-G-A

1502778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25323764-G-C

1502778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25323764-G-T

1502805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25323747-G-A

http://identifiers.org/hco/16/GRCh38#1502979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25323602-C-A

1502979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25323602-C-T

1505386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25322767-G-A

1505390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25322763-C-T

http://identifiers.org/hco/16/GRCh38#1505440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25322713-A-C

1505464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25322689-C-G

1505464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25322689-C-T

1505474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25322679-G-A

1505552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25322601-G-A

1505552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25322601-G-C

1505552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25322601-G-T

1505596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25322557-T-C

1505856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25322169-A-G

1505933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25321945-T-C

http://identifiers.org/hco/16/GRCh38#1506168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25321750-C-A

1506168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25321750-C-T

1506413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25321562-T-C

1506487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 25321502-G-A

1506487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25321502-G-T

1506511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 25321478-T-C

1506545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25321438-C-T

1506624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 25321374-C-T

http://identifiers.org/hco/16/GRCh38#1506645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/17/GRCm39#25321356-C-A

1506645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 25321356-C-T

1506673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25321336-T-C

1506673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25321336-T-G

1506727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25321308-G-A

1506727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25321308-G-T

http://identifiers.org/hco/16/GRCh38#1506750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25321298-C-A

1506750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25321298-C-T

1506751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25321297-C-T

1506835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25321211-G-A

1506835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25321211-G-C

1506835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25321211-G-T

1506867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25321180-C-T

1507032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25321002-G-A

1507064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25320970-A-G

1507084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25320913-G-T

http://identifiers.org/hco/16/GRCh38#1507157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25320814-C-A

1507157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25320814-C-T

1507210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25320761-G-A

1507210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25320761-G-C

1507210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25320761-G-T

http://identifiers.org/hco/16/GRCh38#1507212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25320759-C-A

1507212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25320759-C-G

1507281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25320701-T-C

1507459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25320551-T-C

http://identifiers.org/hco/16/GRCh38#1507469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25320541-C-A

1507469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25320541-C-T

http://identifiers.org/hco/16/GRCh38#1507512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25320510-C-A

1507512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25320510-C-G

1507512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25320510-C-T

1507536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25320475-T-A

1507536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25320475-T-C

1507540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25320471-G-T

1507542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25320469-G-A

1507542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25320469-G-T

1507557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25320438-G-T

1507559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25320436-T-G

1507629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25320358-G-A

1507629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25320358-G-T

1509851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25319071-A-G

1509982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318922-G-A

1509982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318922-G-T

http://identifiers.org/hco/16/GRCh38#1509986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25318918-C-A

1509986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318918-C-G

1509986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318918-C-T

http://identifiers.org/hco/16/GRCh38#1510007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25318901-C-A

1510007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318901-C-T

1510050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318854-G-A

1510050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318854-G-C

1510050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318854-G-T

http://identifiers.org/hco/16/GRCh38#1510101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25318811-C-A

1510101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318811-C-T

1510102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318810-A-T

http://identifiers.org/hco/16/GRCh38#1510105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25318807-C-A

1510105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318807-C-T

http://identifiers.org/hco/16/GRCh38#1510154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#25318755-C-A

1510154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318755-C-T

1510302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318617-G-C

1510302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318617-G-T

1510311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318608-T-C

1510311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318608-T-G

1510372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318539-C-T

1510419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318463-G-A

1510419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25318463-G-T

1510437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29099
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 25318445-T-G