http://identifiers.org/hco/8/GRCh38#123498155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58039546-A-C

123498505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58039876-G-T

http://identifiers.org/hco/8/GRCh38#123498510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58039881-C-A

123498571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58039925-G-T

123498613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58039981-A-G

http://identifiers.org/hco/8/GRCh38#123498814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58040351-C-A

123498817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58040354-T-C

123498818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58040355-A-G

123498847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58040384-C-T

123498956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58040492-G-T

123499076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58040606-G-T

http://identifiers.org/hco/8/GRCh38#123499114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58040644-C-A

123499114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58040644-C-T

123499125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58040657-G-T

http://identifiers.org/hco/8/GRCh38#123499135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58040667-A-C

123499300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58040866-A-G

123499798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58041380-C-T

123499911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58041457-T-A

123499911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58041457-T-C

http://identifiers.org/hco/8/GRCh38#123500032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58041576-C-A

123500280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58041838-C-G

123500332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58041880-G-C

123500332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58041880-G-T

123500511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58042053-T-C

123500861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58042376-A-G

http://identifiers.org/hco/8/GRCh38#123501112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58042614-C-A

http://identifiers.org/hco/8/GRCh38#123501373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58043058-A-C

123501439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58043108-A-G

123501489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58043175-G-A

123501489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58043175-G-T

123501624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58043318-G-A

123501636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58043330-C-T

123501683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58043359-T-C

123501723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58043399-C-T

123501742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58043421-G-T

123502034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58043696-T-C

http://identifiers.org/hco/8/GRCh38#123502156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58043793-A-C

123502157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58043794-G-A

123502157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58043794-G-T

123502243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58043883-G-T

123502286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58043928-G-T

123502299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58043941-A-G

123502356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58044012-G-A

123502547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58044087-T-G

123502562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58044102-T-A

123502562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58044102-T-C

http://identifiers.org/hco/8/GRCh38#123502701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58044215-C-A

123502701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58044215-C-T

123502791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58044299-G-A

123502840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58044348-A-G

123502840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58044348-A-T

123503076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58044568-A-T

123503088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3 prime UTR variant
orthologous variants: 58044580-G-T

123503126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58044618-T-C

123503139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58044636-G-C

123503139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58044636-G-T

123503150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58044647-G-T

123503165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58044663-A-G

123503227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58044725-T-A

123503227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58044725-T-C

123503232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58044730-T-A

123503232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58044730-T-C

123503374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 58044863-C-T

123503472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58044961-A-G

http://identifiers.org/hco/8/GRCh38#123503564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58045033-A-C

123503564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58045033-A-G

123503564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58045033-A-T

123504769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58046402-G-A

123504780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58046426-G-A

123504780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58046426-G-T

http://identifiers.org/hco/8/GRCh38#123504801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58046447-C-A

123504801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58046447-C-T

123504834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58046480-T-A

123504843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58046489-C-T

http://identifiers.org/hco/8/GRCh38#123504854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58046503-C-A

123504854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58046503-C-G

123504890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58046548-T-A

http://identifiers.org/hco/8/GRCh38#123505126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58046750-C-A

123505126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58046750-C-T

123505306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58046923-C-T

123506422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58047508-T-C

123507123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58049235-C-T

123507153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58049272-C-T

123507404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58049467-G-A

123507435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58049499-T-G

123508284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58050317-C-G

123508284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58050317-C-T

123508511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58050547-C-T

123508586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58050609-C-T

123509217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58051237-G-C

123509280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58051299-T-A

123510041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58052105-A-G

123510041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58052105-A-T

123510168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58052255-A-G

123510774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58052586-C-T

123510897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58052719-A-G

123510923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58052744-T-C

123511023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58052830-G-A

123511139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58052949-G-C

http://identifiers.org/hco/8/GRCh38#123511304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58053121-A-C

123511413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58053227-G-T

123511424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58053241-T-A

123512018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58053472-C-T

123512258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58053767-G-A

http://identifiers.org/hco/8/GRCh38#123512457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58053965-A-C

123512462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58053970-T-C

123512553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58054041-T-C

123512901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58054374-C-T

http://identifiers.org/hco/8/GRCh38#123512984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58054450-C-A

123512984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58054450-C-T

http://identifiers.org/hco/8/GRCh38#123513151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58054613-C-A

123513151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58054613-C-G

123513387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 58054870-A-T

123513396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58054878-G-A

123513423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58054905-G-A

123513423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58054905-G-T

123513608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58055058-C-T

123513728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58055181-G-A

123513892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58055329-A-T

http://identifiers.org/hco/8/GRCh38#123513926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58055362-A-C

123513926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58055362-A-G

123513928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58055364-G-C

123513928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58055364-G-T

http://identifiers.org/hco/8/GRCh38#123513977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58055406-A-C

123514099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58055528-T-C

123514124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58055552-T-C

123514178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58055605-G-C

123514178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58055605-G-T

123514186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58055613-A-G

http://identifiers.org/hco/8/GRCh38#123514203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58055630-C-A

123514203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58055630-C-T

http://identifiers.org/hco/8/GRCh38#123514416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#58055851-C-A

123514416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58055851-C-T

123514454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58055960-A-G

http://identifiers.org/hco/8/GRCh38#123514476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58056008-C-A

http://identifiers.org/hco/8/GRCh38#123514510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58056043-C-A

123514691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58056230-C-T

http://identifiers.org/hco/8/GRCh38#123514707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58056246-C-A

123514707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58056246-C-T

123516527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58057323-T-C

123516539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58057335-G-A

123516600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58057389-A-G

http://identifiers.org/hco/8/GRCh38#123516755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#58057538-C-A

123516791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58057574-G-A

123517497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58058339-G-C

123517497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58058339-G-T

123518504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58059479-T-C

http://identifiers.org/hco/8/GRCh38#123518580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58059536-C-A

http://identifiers.org/hco/8/GRCh38#123518706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58059644-C-A

123518800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58059724-G-C

123520234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58060180-T-A

123520349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58060288-T-C

123520351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58060290-G-A

123520351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58060290-G-C

123520517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58060452-T-C

123520749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58060872-A-G

123520833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58060956-T-C

123521117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58061220-A-G

123521475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58061598-T-G

123521604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58061712-G-C

123521627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58061735-G-C

123521667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58061781-G-T

123521818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58062219-C-T

123522207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58062605-T-A

123522207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58062605-T-C

123522207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58062605-T-G

123522209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58062607-T-C

123522234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58062619-G-A

123522234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58062619-G-T

http://identifiers.org/hco/8/GRCh38#123522744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58062832-C-A

123522877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58062963-A-G

123522956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58063023-T-A

123523674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58063331-T-A

123523694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58063354-T-C

123524944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58063584-T-A

123524959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58063601-T-G

123525128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58063757-T-G

123525180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58063814-T-C

123525223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58063864-T-G

123525399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58064037-G-C

123525408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58064046-G-A

123525560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58064191-A-G

123525729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58064718-C-T

123525898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58064866-A-G

123526010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58064988-C-T

http://identifiers.org/hco/8/GRCh38#123526021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58064999-A-C

123526988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58065322-G-A

123527432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58066146-A-G

123527582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58066288-C-T

123527648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58066344-C-T

123527726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58066381-T-A

123527813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58066454-A-G

123527875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58066516-G-A

123527927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58066543-C-T

123527941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58066556-T-C

123528054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58066645-C-T

123529403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58066890-T-A

123529403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58066890-T-C

123529572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58067022-C-T

123529621-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58067069-A-T

123529686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58067146-T-C

123529717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58067173-A-G

123529828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58067269-T-C

123530052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58067489-G-A

123530172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58067608-C-T

123530363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58067789-G-A

123530441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58067864-C-G

123530513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58067938-G-A

123530568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58067993-A-G

123531689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58068367-G-C

123531767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58068447-G-A

123531767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58068447-G-T

123531867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58068580-C-T

123531940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58068651-T-G

123531976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58068687-G-A

http://identifiers.org/hco/8/GRCh38#123532085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58068783-C-A

123532085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58068783-C-T

123532091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58068789-G-A

http://identifiers.org/hco/8/GRCh38#123532150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58068844-C-A

123532150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58068844-C-T

123532181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58068873-C-T

123532350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58069014-G-A

123532587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58069219-C-G

123532587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58069219-C-T

http://identifiers.org/hco/8/GRCh38#123532604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58069236-A-C

123532624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58069255-A-G

123532656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58069287-C-T

123533019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58069498-T-A

123533019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58069498-T-C

123533160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58069565-G-A

123533160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58069565-G-T

123533203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58069607-T-A

123534159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58069939-G-C

123534294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58070079-C-T

123534316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58070097-G-A

123534320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58070101-A-G

123534320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58070101-A-T

123534525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58070810-T-C

123534574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58070837-T-G

123534819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 58071467-G-T

123534892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58071521-T-A

123534892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58071521-T-G

123534919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58071550-G-A

123534919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58071550-G-T

123534934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58071570-T-A

123534934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58071570-T-C

123534934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58071570-T-G

123535044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58071683-A-G

123535170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58071805-G-T

123535619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58072580-T-C

http://identifiers.org/hco/8/GRCh38#123535815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58072945-C-A

123535827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58072957-G-T

http://identifiers.org/hco/8/GRCh38#123535847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58072971-C-A

123535847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58072971-C-T

123535852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58072976-G-A

123535852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58072976-G-C

123535852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58072976-G-T

123535870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58072995-A-T

123536420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58073550-C-G

123536489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58073614-G-A

123536732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58073875-A-G

123536927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58074022-T-G

123537017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58074099-A-G

123537473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58074587-T-C

123537519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58074628-C-T

123538659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58075842-A-G

123538708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58075891-C-T

123538814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58076004-C-G

123539171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58076292-T-G

123539355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58076464-G-T

123539464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58076569-C-G

123539539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58076648-G-A

123539773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58076836-C-T

123539974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58077046-C-T

123540073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58077110-A-G

123540163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58077186-C-G

123540183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58077199-G-A

123540413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58077414-A-G

123540434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58077433-G-T

123540552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58077546-G-C

123540875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58077871-G-A

123540875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58077871-G-C

123540875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58077871-G-T

123540878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58077874-G-T

123541071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 58078079-G-A

123541098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58078110-G-A

123541098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58078110-G-T