32876376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35139141-A-G

32876440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35139083-A-G

32876593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35138978-G-A

32876593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35138978-G-T

32876607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35138970-G-A

32876607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35138970-G-C

32876607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35138970-G-T

32876666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35138922-A-G

http://identifiers.org/hco/19/GRCh38#32876668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35138920-C-A

32876668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35138920-C-T

http://identifiers.org/hco/19/GRCh38#32876697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35138896-C-A

32876697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35138896-C-T

32876717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35138883-T-C

32876727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35138874-T-C

32876730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35138871-G-A

32876730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35138871-G-T

32876876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35138745-T-A

32876972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35138688-G-A

32876972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35138688-G-T

32876979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35138679-G-A

http://identifiers.org/hco/19/GRCh38#32878506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35138483-C-A

32878506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3 prime UTR variant
orthologous variants: 35138483-C-T

http://identifiers.org/hco/19/GRCh38#32878537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35138451-C-A

32878538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3 prime UTR variant
orthologous variants: 35138450-T-C

32878859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3 prime UTR variant
orthologous variants: 35138190-T-G

32878870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3 prime UTR variant
orthologous variants: 35138179-A-G

32878872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3 prime UTR variant
orthologous variants: 35138177-G-A

http://identifiers.org/hco/19/GRCh38#32878943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35138156-C-A

32878947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3 prime UTR variant
orthologous variants: 35138152-G-A

32878951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3 prime UTR variant
orthologous variants: 35138148-G-A

32878951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3 prime UTR variant
orthologous variants: 35138148-G-T

32878976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3 prime UTR variant
orthologous variants: 35138133-A-T

http://identifiers.org/hco/19/GRCh38#32878988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35138121-A-C

32878988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3 prime UTR variant
orthologous variants: 35138121-A-G

32878988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3 prime UTR variant
orthologous variants: 35138121-A-T

http://identifiers.org/hco/19/GRCh38#32879032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35138086-C-A

32879032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35138086-C-T

http://identifiers.org/hco/19/GRCh38#32879074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35138046-C-A

32879074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35138046-C-T

http://identifiers.org/hco/19/GRCh38#32879119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35138008-C-A

32879185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35137941-T-G

32879217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35137909-A-G

32879281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35137848-C-T

32879312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 35137817-T-C

32881824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35135087-G-A

32881824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35135087-G-T

32881886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35135024-T-C

32881886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35135024-T-G

http://identifiers.org/hco/19/GRCh38#32881907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35135003-C-A

32881907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35135003-C-T

32881994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35134916-G-A

32881994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35134916-G-T

32882031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35134881-T-C

http://identifiers.org/hco/19/GRCh38#32882113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35134844-C-A

32882113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35134844-C-G

32882113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35134844-C-T

http://identifiers.org/hco/19/GRCh38#32882119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35134838-A-C

http://identifiers.org/hco/19/GRCh38#32882125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35134832-A-C

32882125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35134832-A-G

32882125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35134832-A-T

32882134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35134823-G-A

32882134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35134823-G-T

32882138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35134819-A-G

32882149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35134808-G-A

32882149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35134808-G-T

32882740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35133878-A-G

http://identifiers.org/hco/19/GRCh38#32887633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35132205-C-A

http://identifiers.org/hco/19/GRCh38#32887652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35132171-C-A

32887652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35132171-C-G

http://identifiers.org/hco/19/GRCh38#32887654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35132169-C-A

32887654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35132169-C-T

http://identifiers.org/hco/19/GRCh38#32887674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35132149-C-A

32887674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35132149-C-G

32887684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35132139-A-G

32887686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35132137-A-T

32887722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35132074-T-C

http://identifiers.org/hco/19/GRCh38#32887728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35132068-C-A

32887728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35132068-C-T

32887731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35132065-T-C

32887735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35132059-G-A

32887735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35132059-G-C

32887735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35132059-G-T

http://identifiers.org/hco/19/GRCh38#32887737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35132057-C-A

32889294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35130710-C-T

32889304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35130700-G-A

32889318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35130685-C-G

32889337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35130666-G-A

32889708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35130397-G-A

32889729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35130377-C-G

32889817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35130301-G-A

32889907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35130242-G-A

32889916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35130233-G-A

32889947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35130192-C-T

http://identifiers.org/hco/19/GRCh38#32899780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35128796-C-A

32899790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35128786-A-T

http://identifiers.org/hco/19/GRCh38#32899804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35128769-C-A

32899804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35128769-C-T

32899948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35128630-A-G

http://identifiers.org/hco/19/GRCh38#32900055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35128523-C-A

32900055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35128523-C-T

32900059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35128519-G-A

32900059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35128519-G-T

32900847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35127886-G-T

32901429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35127607-T-C

http://identifiers.org/hco/19/GRCh38#32915324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35127211-A-C

32915324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35127211-A-T

32915449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35127091-C-T

32915451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35127089-G-A

32915451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35127089-G-C

32915489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 35127051-G-A

32915537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35127008-G-T

32915692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35126735-G-A

32915703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35126724-G-A

32915788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35126634-A-G

32915841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35126582-C-T

32915853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35126572-A-G

http://identifiers.org/hco/19/GRCh38#32917893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35124401-C-A

32917893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35124401-C-T

32917897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35124397-G-T

32917943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35124353-G-T

http://identifiers.org/hco/19/GRCh38#32917960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35124336-A-C

32918223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, splice_donor_variant
orthologous variants: 35124196-C-T

32918236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35124183-G-A

32918236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35124183-G-T

32918335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, stop_gained
orthologous variants: 35124084-G-A

32918340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, splice_acceptor_variant
orthologous variants: 35124079-C-T

32918403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35124018-G-A

32918403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35124018-G-T

http://identifiers.org/hco/19/GRCh38#32918425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35124003-C-A

32918524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35123951-G-A

http://identifiers.org/hco/19/GRCh38#32923326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35122908-C-A

32923326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35122908-C-T

32923327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35122907-C-T

32923333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35122901-A-G

32923343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35122899-T-C

32923348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35122894-A-G

32923373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35122871-A-T

32923453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 35122812-A-G

http://identifiers.org/hco/19/GRCh38#32923574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35122691-C-A

http://identifiers.org/hco/19/GRCh38#32923579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35122664-A-C

32923584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35122659-C-T

32923587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35122656-A-G

32923587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35122656-A-T

32923606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35122638-G-T

32923607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35122637-G-A

32923607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35122637-G-C

32923634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35122608-G-T

32924043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35122326-T-C

32924313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35122187-T-C

32924439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35122078-C-T

http://identifiers.org/hco/19/GRCh38#32924511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35122014-C-A

32924819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35121730-T-C

32925711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35120837-C-T

32925877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35120684-C-T

32926030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35120506-C-T

32926213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35120358-C-G

32926213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35120358-C-T

32926941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35119713-G-C

32926956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35119698-T-C

32926966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35119688-G-A

32926974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35119680-A-G

32931497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35117716-T-C

32931520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35117693-T-C

32931568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35117645-G-A

32933336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35117377-A-G

http://identifiers.org/hco/19/GRCh38#32933411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35117320-C-A

32933411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35117320-C-T

32933413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35117318-G-A

32933413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35117318-G-T

http://identifiers.org/hco/19/GRCh38#32933429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35117303-A-C

32933539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 35117195-T-C

32933560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 35117174-A-G

32933653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 35117081-T-C

32933683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35117052-G-A

32933683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35117052-G-T

32933695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35117031-A-G

32933700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35117028-G-T

32933711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35116978-T-C

32933725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35116964-T-G

http://identifiers.org/hco/19/GRCh38#32933746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35116941-C-A

http://identifiers.org/hco/19/GRCh38#32933757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35116914-A-C

32937338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35116195-C-T

32937380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35116151-C-T

http://identifiers.org/hco/19/GRCh38#32937396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35116135-A-C

32937404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35116127-G-A

32937404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35116127-G-T

http://identifiers.org/hco/19/GRCh38#32937409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35116122-A-C

32937409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35116122-A-T

http://identifiers.org/hco/19/GRCh38#32937413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35116099-C-A

32937413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35116099-C-T

http://identifiers.org/hco/19/GRCh38#32937464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35116053-A-C

32937464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35116053-A-G

32937476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35116041-T-A

32937476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35116041-T-C

32937484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35116029-G-T

32937541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35115976-G-T

32937584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 35115936-C-T

32937591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 35115922-A-G

32937687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35115826-A-G

32939806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35113642-A-G

32939906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35113547-G-A

32939906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35113547-G-C

32939906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35113547-G-T

32939951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35113504-G-A

32939951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35113504-G-T

http://identifiers.org/hco/19/GRCh38#32939954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35113501-C-A

http://identifiers.org/hco/19/GRCh38#32940016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35113480-A-C

32940016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35113480-A-T

32940083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35113421-C-T

32940105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35113397-T-C

32940107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35113393-C-T

32943310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35111427-T-C

32947218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35109539-T-C

32948055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35109300-C-T

32948056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35109299-C-T

http://identifiers.org/hco/19/GRCh38#32948128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35109223-A-C

32948204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35109153-G-A

32948204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35109153-G-T

32953607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 35105226-G-T

32953608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 35105225-A-G

http://identifiers.org/hco/19/GRCh38#32953658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35105175-C-A

http://identifiers.org/hco/19/GRCh38#32953778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35105064-C-A

32953778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35105064-C-T

32954019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35104874-C-G

32957014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35103086-T-A

32957093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35103051-C-G

32958052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102963-C-G

32959716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102712-T-A

32959815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102659-G-A

32959815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102659-G-T

32959839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102648-C-G

32959847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102640-G-A

32959847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102640-G-T

32959854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102635-C-G

32959854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102635-C-T

32959892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 35102599-G-C

32959899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, splice_donor_variant
orthologous variants: 35102592-C-T

http://identifiers.org/hco/19/GRCh38#32959900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35102591-C-A

32959900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 35102591-C-T

http://identifiers.org/hco/19/GRCh38#32960014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35102477-C-A

32960014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35102477-C-T

http://identifiers.org/hco/19/GRCh38#32960119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35102372-C-A

http://identifiers.org/hco/19/GRCh38#32960142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35102363-C-A

32960142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102363-C-T

32960160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102348-G-A

32960165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102343-G-A

32960165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102343-G-T

32960171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102337-G-T

http://identifiers.org/hco/19/GRCh38#32960178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35102330-C-A

32960178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102330-C-T

http://identifiers.org/hco/19/GRCh38#32960187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35102321-C-A

32960187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102321-C-T

32960188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102320-A-G

32960217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35102289-C-T

32960623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35101752-C-G

32960705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35101663-G-A

32960741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35101636-T-G

32960773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35101606-G-A

32966020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097824-A-G

32966022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097822-G-A

32966022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097822-G-T

32966033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097811-G-A

32966033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097811-G-C

32966033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097811-G-T

32966037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097807-G-T

32966045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097799-T-G

32966114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097755-A-T

http://identifiers.org/hco/19/GRCh38#32966117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35097752-C-A

32966117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097752-C-T

32966139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097730-T-G

32966171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097702-T-C

32966171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097702-T-G

32966212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097661-A-G

32966213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097660-T-A

32966213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097660-T-C

32966213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097660-T-G

32966215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097658-A-G

32966245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097636-A-G

32966248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097633-T-C

32966270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097610-A-T

32966298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097582-G-A

32966298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097582-G-T

http://identifiers.org/hco/19/GRCh38#32966321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35097559-C-A

32966321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097559-C-G

32966321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097559-C-T

32966322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097558-A-T

32966325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097555-G-A

32966325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097555-G-T

http://identifiers.org/hco/19/GRCh38#32966336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35097543-A-C

32966336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35097543-A-G

32966426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35097453-G-A

32966468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 35097411-T-C

http://identifiers.org/hco/19/GRCh38#32966517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35097369-C-A

32966525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35097359-T-C

32966542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35097342-G-A

32966542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35097342-G-T

32966553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35097335-G-A

32966553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35097335-G-T

http://identifiers.org/hco/19/GRCh38#32966557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35097331-A-C

http://identifiers.org/hco/19/GRCh38#32966606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35097289-C-A

32966606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35097289-C-T

32966614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35097281-T-G

32966653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35097244-A-G

32966665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35097232-A-G

32966672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35097225-C-T

32971888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 35096577-G-A

32971888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 35096577-G-C

http://identifiers.org/hco/19/GRCh38#32971899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35096555-C-A

32971899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 35096555-C-G

32971899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 35096555-C-T

32971968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35096497-G-T

http://identifiers.org/hco/19/GRCh38#32971970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35096495-C-A

32971970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35096495-C-T

32971972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25907
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35096493-T-C