15421377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3 prime UTR variant
orthologous variants: 32571934-G-A

15421377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3 prime UTR variant
orthologous variants: 32571934-G-T

15421431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3 prime UTR variant
orthologous variants: 32571994-T-C

15421487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3 prime UTR variant
orthologous variants: 32572049-C-T

15421503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3 prime UTR variant
orthologous variants: 32572065-C-T

15421545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3 prime UTR variant
orthologous variants: 32572102-A-G

http://identifiers.org/hco/19/GRCh38#15421546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32572103-A-C

15421876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3 prime UTR variant
orthologous variants: 32572852-G-A

15421876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3 prime UTR variant
orthologous variants: 32572852-G-T

http://identifiers.org/hco/19/GRCh38#15422020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32572953-C-A

http://identifiers.org/hco/19/GRCh38#15422048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32572989-C-A

15422048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3 prime UTR variant
orthologous variants: 32572989-C-T

15422257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573197-G-A

15422257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573197-G-T

15422360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573301-C-T

http://identifiers.org/hco/19/GRCh38#15422419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573347-C-A

15422419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573347-C-T

http://identifiers.org/hco/19/GRCh38#15422426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573354-C-A

15422426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573354-C-T

15422433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573361-G-A

http://identifiers.org/hco/19/GRCh38#15422436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573364-C-A

15422436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573364-C-T

http://identifiers.org/hco/19/GRCh38#15422455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573383-C-A

15422486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573422-G-A

15422486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573422-G-T

http://identifiers.org/hco/19/GRCh38#15422490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573426-C-A

http://identifiers.org/hco/19/GRCh38#15422491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573427-A-C

15422502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573438-A-G

15422502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573438-A-T

15422510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573445-G-A

15422510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573445-G-T

http://identifiers.org/hco/19/GRCh38#15422519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573454-C-A

15422519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573454-C-T

http://identifiers.org/hco/19/GRCh38#15422525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573460-C-A

15422525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573460-C-G

15422525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573460-C-T

15422527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573462-G-A

15422527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573462-G-C

15422527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573462-G-T

15422550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573484-T-C

15422556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573490-G-T

15422567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573501-G-A

15422567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573501-G-C

http://identifiers.org/hco/19/GRCh38#15422571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573505-C-A

15422571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573505-C-G

15422571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573505-C-T

15422573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573507-T-C

15422573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573507-T-G

15422575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573509-A-T

15422583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573517-G-A

15422583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573517-G-C

15422583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573517-G-T

15422610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573545-G-A

15422611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573546-C-T

15422626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573561-A-G

15422626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573561-A-T

15422639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573575-T-C

15422639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573575-T-G

15422646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573582-G-A

15422646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573582-G-C

15422651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573587-C-T

15422654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573590-G-A

15422654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573590-G-T

15422661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573593-T-C

15422661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573593-T-G

15422666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573598-G-A

15422666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573598-G-T

15422675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573607-T-C

15422732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573658-C-T

15422744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573670-A-G

http://identifiers.org/hco/19/GRCh38#15422749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573675-C-A

15422749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573675-C-G

15422749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573675-C-T

http://identifiers.org/hco/19/GRCh38#15422776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573704-C-A

15422776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573704-C-T

http://identifiers.org/hco/19/GRCh38#15422797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573725-C-A

15422801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573729-C-T

http://identifiers.org/hco/19/GRCh38#15422808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573736-C-A

15422816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573744-T-C

http://identifiers.org/hco/19/GRCh38#15422825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573753-C-A

15422825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 32573753-C-T

15422830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 32573758-G-T

http://identifiers.org/hco/19/GRCh38#15422831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573759-C-A

15422831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 32573759-C-T

15422833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 32573761-G-A

15422833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 32573761-G-T

15422855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573781-A-G

15422855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573781-A-T

15422871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573795-G-A

15422871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573795-G-T

http://identifiers.org/hco/19/GRCh38#15422874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573798-C-A

15422874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573798-C-T

http://identifiers.org/hco/19/GRCh38#15422875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573799-C-A

15422875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573799-C-G

15422891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573815-G-A

15422891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573815-G-T

15422897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573821-G-A

15422897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573821-G-T

15422910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573834-G-A

15422910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573834-G-T

http://identifiers.org/hco/19/GRCh38#15422921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573845-C-A

15422921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573845-C-T

http://identifiers.org/hco/19/GRCh38#15422922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573846-C-A

15422922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573846-C-T

15422923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573847-T-C

15422929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573853-T-C

15422929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573853-T-G

http://identifiers.org/hco/19/GRCh38#15422936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573860-C-A

15422936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573860-C-T

http://identifiers.org/hco/19/GRCh38#15422937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573861-C-A

15422939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573863-G-A

15422939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573863-G-T

15422940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573864-G-A

15422940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573864-G-C

15422940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573864-G-T

http://identifiers.org/hco/19/GRCh38#15422952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573876-C-A

15422952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573876-C-T

15422953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573877-G-A

15422953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573877-G-T

15422956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573880-G-A

15422956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573880-G-T

15422960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573884-T-C

http://identifiers.org/hco/19/GRCh38#15422975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573899-C-A

15422975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573899-C-T

http://identifiers.org/hco/19/GRCh38#15422977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573901-C-A

15422977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573901-C-G

15422977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573901-C-T

http://identifiers.org/hco/19/GRCh38#15422978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573902-C-A

http://identifiers.org/hco/19/GRCh38#15422987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573911-C-A

15422987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573911-C-T

http://identifiers.org/hco/19/GRCh38#15422995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32573920-A-C

15422999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573924-G-C

15422999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573924-G-T

15423016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573941-A-G

15423016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573941-A-T

15423019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573944-G-T

15423021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573946-G-A

15423021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573946-G-C

15423021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573946-G-T

15423028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573953-G-A

15423028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 32573953-G-T

15423090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 32574012-C-T

15423110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 32574032-G-A

15423110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 32574032-G-C

15423112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 32574034-G-T

http://identifiers.org/hco/19/GRCh38#15423114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32574036-C-A

15423119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 32574041-G-A

15423119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 32574041-G-C

15423129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 32574051-G-A

15423130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 32574052-T-C

15423130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 32574052-T-G

15423132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 32574054-G-A

15423132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 32574054-G-C

15423132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 32574054-G-T

15423352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32574271-G-A

15423352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32574271-G-C

15423352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32574271-G-T

15423416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32574320-T-C

15423416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32574320-T-G

15423568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32574431-A-T

15423748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32574803-A-G

15423795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32574874-T-C

15423983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32575184-G-A

15423983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32575184-G-T

15423988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32575189-A-G

http://identifiers.org/hco/19/GRCh38#15424074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32575311-C-A

15424074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32575311-C-T

15424084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32575322-G-A

http://identifiers.org/hco/19/GRCh38#15424145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32575380-C-A

http://identifiers.org/hco/19/GRCh38#15424147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32575382-C-A

15424147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32575382-C-G

15424147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32575382-C-T

15424275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32575489-T-C

15424275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32575489-T-G

15424459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32575682-A-G

15424478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32575694-G-A

15424563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32575773-G-A

15424563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32575773-G-T

15424833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32576083-G-A

15425205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32576395-G-A

15425205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32576395-G-T

15425218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32576408-G-A

15425382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 32576572-T-C

15425438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 32576628-G-T

http://identifiers.org/hco/19/GRCh38#15425440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32576630-C-A

15425440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 32576630-C-G

15425440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 32576630-C-T

http://identifiers.org/hco/19/GRCh38#15425502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32576692-C-A

15425502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 32576692-C-G

15425502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 32576692-C-T

15426086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32577180-C-T

http://identifiers.org/hco/19/GRCh38#15426197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32577293-A-C

15426305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32577369-G-A

15426401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32577465-C-T

http://identifiers.org/hco/19/GRCh38#15426558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32577597-A-C

15426559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32577598-C-G

http://identifiers.org/hco/19/GRCh38#15426854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32577794-C-A

15426854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32577794-C-T

15426885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32577820-T-C

http://identifiers.org/hco/19/GRCh38#15426961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32577896-C-A

15427272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 32578207-C-G

15427964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32578859-T-A

15428414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 32579307-G-A

15428652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32579599-T-G

15429016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32579889-C-T

15429096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32579967-G-A

15429240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32580125-G-A

15429359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32580237-G-A

15429453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32580327-G-A

15429453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32580327-G-T

15429465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32580339-G-A

15429465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32580339-G-T

15429471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32580345-T-C

15429471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32580345-T-G

http://identifiers.org/hco/19/GRCh38#15429474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32580349-A-C

15429474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32580349-A-G

15429474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32580349-A-T

http://identifiers.org/hco/19/GRCh38#15429539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32580392-C-A

15429539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32580392-C-G

15429539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32580392-C-T

http://identifiers.org/hco/19/GRCh38#15429544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32580397-C-A

http://identifiers.org/hco/19/GRCh38#15429853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32580702-C-A

15429853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 32580702-C-G

http://identifiers.org/hco/19/GRCh38#15430214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32581052-C-A

15430214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32581052-C-T

15430304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32581138-G-C

15430455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32581297-C-G

http://identifiers.org/hco/19/GRCh38#15430541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32581366-C-A

15430563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32581388-C-T

15430952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32581734-G-A

15430952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32581734-G-T

15431702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32582407-G-A

http://identifiers.org/hco/19/GRCh38#15431840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32582539-C-A

15432245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32582975-G-A

15432323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32583042-T-C

15432323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32583042-T-G

http://identifiers.org/hco/19/GRCh38#15432409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32583131-C-A

15432409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32583131-C-T

15432516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 32583238-T-A

15432516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 32583238-T-C

15432516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 32583238-T-G

http://identifiers.org/hco/19/GRCh38#15432552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32583262-C-A

15432552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 32583262-C-G

15432552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 32583262-C-T

15432896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32583568-G-A

15432937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32583599-G-A

15433019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32583681-G-A

15433019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32583681-G-T

http://identifiers.org/hco/19/GRCh38#15433087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32583753-C-A

15433242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 32583970-T-C

15433308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32584048-G-A

15433308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32584048-G-T

15433345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32584093-C-T

http://identifiers.org/hco/19/GRCh38#15433346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32584094-A-C

15433347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32584095-T-C

15433347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32584095-T-G

15433439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32584191-G-T

http://identifiers.org/hco/19/GRCh38#15433487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32584237-A-C

15433726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32584654-G-T

15433933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32584768-G-A

15436408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32586347-A-G

15436434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32586375-A-G

15436434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32586375-A-T

http://identifiers.org/hco/19/GRCh38#15436521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32586457-C-A

15436521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32586457-C-T

http://identifiers.org/hco/19/GRCh38#15436546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32586477-C-A

15436548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32586479-G-A

15436548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32586479-G-C

http://identifiers.org/hco/19/GRCh38#15436591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32586487-C-A

15436591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32586487-C-G

15436637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32586533-G-A

15436693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32586607-G-A

15436693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32586607-G-C

15436693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32586607-G-T

15436701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32586699-A-G

15436702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32586700-T-A

15436702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32586700-T-C

15436726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32586724-G-A

15436726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32586724-G-T

15436945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32586937-A-G

15436954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32586946-G-A

15437290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32587307-C-T

15437344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32587365-G-A

15437994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32587675-G-C

15438037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32587715-T-C

15438106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32587769-A-T

15438328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32587970-G-A

15438341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32587984-T-G

http://identifiers.org/hco/19/GRCh38#15438456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32588104-C-A

http://identifiers.org/hco/19/GRCh38#15438458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32588106-A-C

15438458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32588106-A-G

15438458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32588106-A-T

15438687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32588370-C-T

http://identifiers.org/hco/19/GRCh38#15438773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32595557-C-A

15438846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32595630-G-T

http://identifiers.org/hco/19/GRCh38#15438963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32595750-C-A

15438963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 32595750-C-T

15439532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 32596301-C-G

15439532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 32596301-C-T

http://identifiers.org/hco/19/GRCh38#15439536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32596305-C-A

15439536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 32596305-C-T

http://identifiers.org/hco/19/GRCh38#15439857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32596617-C-A

15439965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 32596725-C-T

http://identifiers.org/hco/19/GRCh38#15440010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32596770-C-A

15440010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 32596770-C-G

15440010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 32596770-C-T

15440244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 32597001-G-A

15440244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 32597001-G-T

15440249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 32597006-G-A

15440349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 32597106-G-A

http://identifiers.org/hco/19/GRCh38#15440399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32597156-C-A

15440399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 32597156-C-T

15440641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 32597398-G-A

15440641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 32597398-G-T

15440785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32597546-G-A

15440785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32597546-G-T

http://identifiers.org/hco/19/GRCh38#15440821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32597586-C-A

15440821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32597586-C-T

http://identifiers.org/hco/19/GRCh38#15440836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32597606-C-A

15440836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32597606-C-T

http://identifiers.org/hco/19/GRCh38#15442528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32599913-C-A

15442528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32599913-C-T

http://identifiers.org/hco/19/GRCh38#15442859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32600262-C-A

15442859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32600262-C-T

http://identifiers.org/hco/19/GRCh38#15442870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32600271-C-A

15442870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32600271-C-T

15442891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32600292-G-C

15442891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32600292-G-T

15442970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32600367-C-T

15443079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32600473-T-C

15443083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32600477-A-G

15443165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32600612-G-T

http://identifiers.org/hco/19/GRCh38#15443553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32601291-C-A

15443553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32601291-C-T

15444155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32601850-A-T

15444547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32602218-A-G

15445180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32602801-G-A

15445453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32603069-G-A

15445737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32603318-G-C

15446049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32603617-T-G

15446191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32603757-C-T

15446271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32603844-G-A

15446923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32604278-G-A

15447063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32605594-G-A

15447303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32605821-G-A

15447349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32605868-G-A

15447844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32606309-G-A

15447985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32606432-G-A

15447985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32606432-G-T

http://identifiers.org/hco/19/GRCh38#15447987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32606435-C-A

15447987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32606435-C-T

15448030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32606478-G-A

15448068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32606516-A-T

15448415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32606838-C-G

15448415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32606838-C-T

15448479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32606901-C-T

15448558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32606984-C-G

http://identifiers.org/hco/19/GRCh38#15448652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32607071-C-A

15448755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32607166-C-T

15448868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32607265-C-T

15449063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32607444-C-T

15449236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32607646-G-C

15449497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32607933-G-A

15449720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32608158-C-G

15449720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30917
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32608158-C-T