19351573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18774816-T-C

19351645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18774752-A-T

19351675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18774722-T-C

19351807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18774583-C-T

http://identifiers.org/hco/22/GRCh38#19352193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18774269-C-A

19352308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18774200-C-G

19352384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18774125-T-G

19352538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18774031-C-T

19352674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18773941-T-C

19352701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18773915-G-A

19352748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18773843-A-G

19352825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18773743-T-C

19352846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18773722-T-A

19352846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18773722-T-G

19352848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18773720-C-T

19352876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18773692-T-C

http://identifiers.org/hco/22/GRCh38#19353499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18773378-C-A

19353499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18773378-C-T

19353878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18772950-G-A

19353878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18772950-G-C

19353878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18772950-G-T

19354053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18772808-G-A

http://identifiers.org/hco/22/GRCh38#19354209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18772690-C-A

http://identifiers.org/hco/22/GRCh38#19354257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18772644-C-A

19354532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18772264-T-G

http://identifiers.org/hco/22/GRCh38#19354540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18772256-C-A

19354599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18772196-A-T

http://identifiers.org/hco/22/GRCh38#19354762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18771947-C-A

19354792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18771922-G-C

19355240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18771786-G-A

19355304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18771316-C-T

http://identifiers.org/hco/22/GRCh38#19355612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18771032-C-A

19355612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18771032-C-T

19355666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18770999-G-T

http://identifiers.org/hco/22/GRCh38#19355690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18770984-C-A

19355695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18770977-T-C

19355698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18770974-T-C

19356041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18770637-C-T

19356058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18770618-T-C

19356207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18770486-G-C

19356360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18770343-G-A

19356368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18770335-G-A

19356369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18770334-G-A

19356369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18770334-G-T

19356371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18770332-C-T

http://identifiers.org/hco/22/GRCh38#19356375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18770330-C-A

19356375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18770330-C-T

19356388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18770317-T-A

19356388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18770317-T-G

19356810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18770145-T-C

19356935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 18770039-C-G

19356935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 18770039-C-T

19357152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18769844-G-A

19357152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18769844-G-C

19357153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18769843-G-T

19357163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18769824-G-C

19357163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18769824-G-T

19357443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18769549-A-T

19357461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18769533-G-A

19357475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18769519-G-A

19357508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18769468-G-T

19357647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18769351-A-T

19357792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18769265-G-C

http://identifiers.org/hco/22/GRCh38#19357905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18769178-A-C

19357960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18769129-A-G

19358231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18769083-C-T

http://identifiers.org/hco/22/GRCh38#19358871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18768369-C-A

19358973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18768264-G-A

19359125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18768167-G-T

http://identifiers.org/hco/22/GRCh38#19359229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18768094-A-C

http://identifiers.org/hco/22/GRCh38#19359270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18768072-C-A

19359270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18768072-C-G

http://identifiers.org/hco/22/GRCh38#19359310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18768043-C-A

19359310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18768043-C-T

19359423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 18767945-A-G

19359560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18767833-T-A

19359560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18767833-T-C

19359630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18767764-G-A

19359630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18767764-G-T

19359807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18767691-G-C

19360399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18767216-G-A

19360505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18767155-C-T

19360660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18767006-C-T

19360680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18766986-C-T

http://identifiers.org/hco/22/GRCh38#19360945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18766526-C-A

http://identifiers.org/hco/22/GRCh38#19361128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18766366-C-A

19361143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18766351-T-G

19361180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18766319-G-A

19361180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18766319-G-T

19361386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18766116-G-T

http://identifiers.org/hco/22/GRCh38#19361705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18765316-A-C

19361886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 18765139-G-C

http://identifiers.org/hco/22/GRCh38#19361887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18765138-A-C

19361887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 18765138-A-T

19361893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 18765132-C-T

19361895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 18765130-G-A

19361895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 18765130-G-C

19361915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 18765110-G-A

19361915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 18765110-G-C

19361920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 18765105-T-C

19375400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18754084-T-C

19375540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18753976-G-A

19375540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18753976-G-T

19375811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18753750-G-C

19375815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18753746-C-G

19375848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18753713-T-A

http://identifiers.org/hco/22/GRCh38#19375872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18753689-C-A

19375872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18753689-C-T

19375928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18753634-A-T

19376255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18753315-G-A

19376388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18753241-T-C

19376471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18753168-A-G

19376511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18753122-G-A

19376628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18753025-G-A

http://identifiers.org/hco/22/GRCh38#19376671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18752992-C-A

19376671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18752992-C-T

19377055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18752721-G-A

19377076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18752700-C-T

19377729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18752138-T-A

19377839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18751840-G-A

19377839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18751840-G-T

19377906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18751773-T-C

19378022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18751660-G-C

19378022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18751660-G-T

http://identifiers.org/hco/22/GRCh38#19378200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18751503-A-C

19378691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18751064-G-A

19381263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18748687-T-C

19381485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18748442-T-G

19381740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18747981-T-C

19381831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18747887-A-G

19381963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18747729-A-G

19382445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18747329-G-T

19382833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18747025-A-G

http://identifiers.org/hco/22/GRCh38#19382992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18746866-A-C

http://identifiers.org/hco/22/GRCh38#19383051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18746807-C-A

19383296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18746578-T-A

19383296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18746578-T-C

19383300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18746574-A-T

19383556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18746340-A-T

19384675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18745491-G-T

19384807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18745359-C-T

http://identifiers.org/hco/22/GRCh38#19384855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18745271-A-C

19384856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18745270-T-C

19385002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18745114-A-G

19385051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18745070-G-A

http://identifiers.org/hco/22/GRCh38#19385374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18744782-C-A

19385374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18744782-C-T

19385508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18744624-G-C

19385508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18744624-G-T

19385615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18744517-T-G

19385759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18744372-G-C

19385759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18744372-G-T

19385804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18744327-A-T

19385869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18744260-G-A

19385869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18744260-G-C

19385869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18744260-G-T

19386565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18743591-G-A

19387302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18742106-T-C

http://identifiers.org/hco/22/GRCh38#19387606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18741779-C-A

19387634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18741762-T-A

19387634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18741762-T-C

19387977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18741485-G-A

19387977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18741485-G-C

19387977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18741485-G-T

19388570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18741050-C-T

http://identifiers.org/hco/22/GRCh38#19388647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18740972-C-A

19388802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18740845-C-T

http://identifiers.org/hco/22/GRCh38#19389330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18740006-C-A

19389568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18739791-C-T

19390010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18738934-T-A

http://identifiers.org/hco/22/GRCh38#19390023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18738921-A-C

19390204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18738761-T-G

19391900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18738039-C-T

http://identifiers.org/hco/22/GRCh38#19391954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18737993-C-A

19391954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18737993-C-T

http://identifiers.org/hco/22/GRCh38#19392065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18737864-C-A

19392065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18737864-C-T

19392114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18737824-G-A

19392883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18736523-G-A

19392883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18736523-G-C

19393246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18736217-C-T

19393295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18736170-T-C

19393318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18736142-A-G

19393716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18736058-T-G

19393808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18735969-C-T

19393847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18735930-A-G

19394143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18735636-T-A

http://identifiers.org/hco/22/GRCh38#19394219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18735559-A-C

http://identifiers.org/hco/22/GRCh38#19394626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18735087-C-A

19395772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18734100-G-A

19396569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18731113-G-A

19396578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18731105-C-T

19396663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18731056-G-A

19396663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18731056-G-T

19396681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18731042-T-C

http://identifiers.org/hco/22/GRCh38#19396699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18731026-C-A

19396699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18731026-C-T

19396704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18731021-G-A

19396704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18731021-G-T

19396983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18730748-T-C

19396985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18730722-A-T

19397009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18730702-G-A

19397009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18730702-G-T

19397195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18730456-G-A

19397246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18730414-C-T

19397352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18730307-C-T

19397365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18730294-T-C

19397375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18730284-T-C

19397419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18730241-C-T

19397791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18729726-A-G

http://identifiers.org/hco/22/GRCh38#19397923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18729588-C-A

19397923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18729588-C-T

19397977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18729505-G-C

19397977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18729505-G-T

19397986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18729497-C-G

19397986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18729497-C-T

19398133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18729329-G-T

19398263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18729197-C-T

19398286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18729173-T-G

19398569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18728914-T-A

19398569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18728914-T-C

19399088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18728494-C-T

19399150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18728397-C-T

19399349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18728253-A-T

19399353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18728249-G-T

19399560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18727970-C-T

19399651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18727880-T-A

19399651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18727880-T-C

http://identifiers.org/hco/22/GRCh38#19399978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18727604-C-A

19400309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18727173-G-C

http://identifiers.org/hco/22/GRCh38#19400371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18727112-C-A

19400423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18727072-A-G

19400423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18727072-A-T

19400448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18727047-C-G

19400630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18726868-C-T

19400651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18726812-T-C

http://identifiers.org/hco/22/GRCh38#19400759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18726554-A-C

19404172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18720963-A-G

http://identifiers.org/hco/22/GRCh38#19404300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18720842-C-A

19404320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18720822-G-A

19404354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18720773-A-G

19405350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718997-C-T

19405391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718954-A-T

19405424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718685-T-C

19405432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718677-G-A

19405432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718677-G-T

19405516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718610-C-T

19405533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718593-T-C

19405717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718389-A-G

http://identifiers.org/hco/22/GRCh38#19405718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18718388-C-A

19405718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718388-C-T

19405724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718382-G-A

19405724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718382-G-T

19405889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718102-G-A

19405935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718056-G-A

19405935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718056-G-T

19405969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718021-C-T

19405971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718019-G-A

19405971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718019-G-C

19405971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718019-G-T

19405975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718016-A-T

http://identifiers.org/hco/22/GRCh38#19405985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18718006-C-A

19405985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18718006-C-T

19406030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18717963-G-T

http://identifiers.org/hco/22/GRCh38#19406085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18717905-C-A

19406127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18717860-A-G

19406492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18717288-G-A

19406706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18717013-C-G

19406719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18716995-T-C

19406891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18716830-T-G

19406945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18716781-T-C

19409700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18714460-T-C

19410383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18714030-C-T

19410501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18713902-C-T

http://identifiers.org/hco/22/GRCh38#19410529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18713876-C-A

19410653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18713636-A-G

19410674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18713615-C-T

19410679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18713610-C-T

19410848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18713358-A-G

19410914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18713296-G-A

19410914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18713296-G-T

19410937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18713273-G-A

19411040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18713188-G-A

19411187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18713041-G-C

19411225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18713003-G-A

19411313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18712376-A-G

19411495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18712226-G-C

19411522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18712189-G-T

19411777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18712029-G-A

19411997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18711806-A-G

http://identifiers.org/hco/22/GRCh38#19412491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18709686-A-C

19412842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18709396-T-C

19412866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18709372-T-C

19414047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18708244-G-T

19423613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18703958-C-G

19424219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18701751-C-T

19424783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18701095-T-G

19425201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18700658-A-G

http://identifiers.org/hco/22/GRCh38#19425373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18700509-A-C

19425428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18700455-G-C

19425579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18700303-C-T

19428169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18698601-T-C

http://identifiers.org/hco/22/GRCh38#19428505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18698319-A-C

19428950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18698053-T-C

19430498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18697117-T-C

19430578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18697073-T-C

19430597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18697061-T-A

19430597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18697061-T-G

19430603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18697057-G-T

19430671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18696987-C-T

http://identifiers.org/hco/22/GRCh38#19430672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18696986-C-A

19430672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18696986-C-G

19430672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18696986-C-T

19430757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18696916-A-G

19431032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18696664-C-T

19431119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18696577-G-A

19431119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18696577-G-C

http://identifiers.org/hco/22/GRCh38#19431328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18696377-C-A

19431328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18696377-C-T

19431490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18696217-C-T

19431543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18696170-G-A

19431543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18696170-G-T

19431549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18696167-G-A

19431549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18696167-G-C

19431549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18696167-G-T

http://identifiers.org/hco/22/GRCh38#19431629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18696088-C-A

19431629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18696088-C-T

19431889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695836-G-A

19431904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695816-T-G

19431945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695783-G-A

19431974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695758-T-C

19432086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695634-C-T

19432125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695600-G-A

19432125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695600-G-T

19432227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695488-G-A

19432247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695476-G-A

19432247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695476-G-T

19432377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695452-C-T

http://identifiers.org/hco/22/GRCh38#19432380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18695449-C-A

19432380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695449-C-G

19432380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695449-C-T

19432381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695448-G-A

19432381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695448-G-C

19432381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695448-G-T

19432421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695418-G-A

19432421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695418-G-T

19432436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695403-G-A

19432436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695403-G-C

19432482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695356-T-C

19432482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695356-T-G

19432483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695355-G-A

19432483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695355-G-T

19432494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695344-G-A

19432494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695344-G-T

http://identifiers.org/hco/22/GRCh38#19432544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18695282-C-A

19432544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18695282-C-T

19432550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18695276-T-C

19432560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 18695266-G-A

19432560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 18695266-G-C

19432560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 18695266-G-T

http://identifiers.org/hco/22/GRCh38#19432566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18695260-C-A

19432566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 18695260-C-G

19432566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 18695260-C-T

19432617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18695209-G-A

19432617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18695209-G-T

19432663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18695168-G-A

19432663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18695168-G-C

19432663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18695168-G-T

19432724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18695130-G-A

19432724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18695130-G-T

19432742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18695115-G-A

19432742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18695115-G-C

19432763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18695094-C-T

http://identifiers.org/hco/22/GRCh38#19433287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18694133-C-A

http://identifiers.org/hco/22/GRCh38#19433357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18694063-C-A

19433362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18694059-G-A

19433362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18694059-G-C

19433362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18694059-G-T

19433371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18694050-A-G

http://identifiers.org/hco/22/GRCh38#19433391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18694030-C-A

19433391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18694030-C-T

http://identifiers.org/hco/22/GRCh38#19433395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18694025-C-A

19433512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18693905-C-G

19434560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18692579-C-G

19434560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18692579-C-T

19434609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18692551-T-C

19434677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18692475-C-G

http://identifiers.org/hco/22/GRCh38#19434749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18692430-C-A

19434749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained, undefined
orthologous variants: 18692430-C-T

19434761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 18692418-A-G

19434926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18692255-A-G

19434981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18692207-A-G

19434988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18692200-T-C

19435085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18692131-G-A

19435085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18692131-G-T

19435488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18691590-G-A

19435488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18691590-G-C

19435559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18691520-T-C

http://identifiers.org/hco/22/GRCh38#19435622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18691448-C-A

http://identifiers.org/hco/22/GRCh38#19435642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#18691406-C-A

19435642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 18691406-C-T

19435737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 18691311-G-A

19435817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 18691231-C-G

19435960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, stop_lost, undefined
orthologous variants: 18691085-T-C

19435960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, stop_lost, undefined
orthologous variants: 18691085-T-G

19436142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18690920-T-C

19436168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18690897-A-G

19436172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18690886-C-T

19436263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18690811-G-A

19437154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18690259-A-G

19437164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18690249-G-A

19437505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18689979-C-T

19437589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18689911-T-A

http://identifiers.org/hco/22/GRCh38#19443732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18658448-C-A

19443732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18658448-C-T

http://identifiers.org/hco/22/GRCh38#19443785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18658394-A-C

19443785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18658394-A-G

http://identifiers.org/hco/22/GRCh38#19443799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18658379-C-A

http://identifiers.org/hco/22/GRCh38#19443822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18658358-C-A

19443822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18658358-C-T

19443940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18658236-G-C

19443940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18658236-G-T

http://identifiers.org/hco/22/GRCh38#19443943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18658233-A-C

19443943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18658233-A-G

http://identifiers.org/hco/22/GRCh38#19443964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18658212-C-A

http://identifiers.org/hco/22/GRCh38#19443998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18658155-C-A

19443998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18658155-C-G

19443998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18658155-C-T

19444028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18658125-C-T

http://identifiers.org/hco/22/GRCh38#19444031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18658122-C-A

19444031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18658122-C-T

http://identifiers.org/hco/22/GRCh38#19444087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18658073-C-A

19444104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18658058-G-A

19444104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18658058-G-C

19444251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18657983-G-A

19444251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18657983-G-T

http://identifiers.org/hco/22/GRCh38#19444450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18657758-C-A

19444450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18657758-C-T

http://identifiers.org/hco/22/GRCh38#19444537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18657678-C-A

19444976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18657247-T-G

http://identifiers.org/hco/22/GRCh38#19447185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18655734-C-A

http://identifiers.org/hco/22/GRCh38#19447365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18655632-C-A

19447365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18655632-C-T

http://identifiers.org/hco/22/GRCh38#19447369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18655628-C-A

19447369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18655628-C-G

19447553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 18655446-G-A

19447553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 18655446-G-C

19447553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 18655446-G-T

http://identifiers.org/hco/22/GRCh38#19447615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18655404-C-A

http://identifiers.org/hco/22/GRCh38#19447625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18655394-A-C

http://identifiers.org/hco/22/GRCh38#19447672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#18655360-C-A

19447672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27012
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 18655360-C-G