24583939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 20853074-T-C

24584112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 20853234-G-T

24584168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 20853286-A-T

24584209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 20853327-G-A

24584209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 20853327-G-T

24584409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 20853514-A-G

24584469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20853574-T-C

24584471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 20853576-G-A

24584473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20853578-G-A

24584474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20853579-C-T

24584717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20853828-G-A

24584811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20853922-C-T

24584847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20853958-G-A

24584847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20853958-G-C

24584913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20854024-A-G

24584961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20854072-A-G

24585195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20854306-G-A

24585195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20854306-G-C

24585258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20854369-G-A

24585309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20854420-T-C

24585333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20854444-C-T

24585353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20854464-T-C

24585384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20854495-G-A

24585384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20854495-G-C

24585384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20854495-G-T

24585426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20854537-G-A

24585710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20854818-T-A

24585710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20854818-T-C

24585776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20854884-G-A

24585776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20854884-G-T

24585778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20854886-G-A

24585793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20854901-G-A

24585796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20854904-G-A

24585796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20854904-G-T

24585934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20855024-T-C

24586032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20855122-G-A

http://identifiers.org/hco/10/GRCh38#24586065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20855155-C-A

24586065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20855155-C-G

24586065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20855155-C-T

24586117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20855207-A-G

24586118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20855208-G-T

24586152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20855235-T-C

24586184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20855256-A-G

24586232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20855302-T-A

24586563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20855686-G-A

24586690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20855794-C-G

24586713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20855817-T-C

24586760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20855863-A-T

24587387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20856082-T-A

24587387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20856082-T-C

24587831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20856433-T-A

24587840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20856442-C-G

24587930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20856509-G-A

24588287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20856940-A-T

24589143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20857724-T-C

24589153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20857738-A-T

http://identifiers.org/hco/10/GRCh38#24589156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20857741-C-A

24589156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20857741-C-G

24589156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20857741-C-T

http://identifiers.org/hco/10/GRCh38#24589204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20857781-C-A

24589204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20857781-C-T

http://identifiers.org/hco/10/GRCh38#24589241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20857818-A-C

24589257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20857835-A-G

24589257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20857835-A-T

24589335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20857912-T-A

24589335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20857912-T-C

http://identifiers.org/hco/10/GRCh38#24589803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20858369-C-A

24589803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20858369-C-T

24589844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20858412-G-T

http://identifiers.org/hco/10/GRCh38#24589890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20858453-C-A

24589890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20858453-C-T

24589897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20858460-G-A

24589897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20858460-G-T

http://identifiers.org/hco/10/GRCh38#24590020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20858582-C-A

24590478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 20859042-G-A

24590478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 20859042-G-T

24590590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20859154-A-G

24590597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20859161-T-A

http://identifiers.org/hco/10/GRCh38#24590610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20859174-C-A

24590610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20859174-C-T

24590641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20859203-A-G

24590662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20859224-A-G

http://identifiers.org/hco/10/GRCh38#24590895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20859418-A-C

24590895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20859418-A-G

24590945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20859468-A-T

24590996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20859514-T-C

24590996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20859514-T-G

24591037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20859555-A-T

24591067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20859579-G-T

http://identifiers.org/hco/10/GRCh38#24591115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20859632-A-C

24591191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20859703-G-A

24591191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20859703-G-T

24591199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20859711-G-A

24591378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20859899-T-A

24591378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20859899-T-G

24591612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20860141-T-C

24591618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20860147-C-T

24591750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20860275-T-A

24591750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20860275-T-C

24591750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20860275-T-G

24591767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20860292-A-G

24591779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20860306-G-A

24591779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20860306-G-T

24591786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20860313-A-G

24591839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20860365-T-C

http://identifiers.org/hco/10/GRCh38#24591855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20860381-C-A

24592857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20860910-G-A

24592917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20860966-T-C

24593233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20861410-G-T

24593269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20861446-A-G

24593309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20861474-T-C

24593525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20861674-G-A

24594051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20862773-T-G

http://identifiers.org/hco/10/GRCh38#24594095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20862819-C-A

24594100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20862824-A-G

24594616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20863397-T-C

24594800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20863581-T-C

24594820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20863599-T-A

24594820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20863599-T-C

24594820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20863599-T-G

24594860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20863632-T-A

24594860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20863632-T-C

24594860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20863632-T-G

24594880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20863652-G-T

24594916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20863674-A-G

24594916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20863674-A-T

http://identifiers.org/hco/10/GRCh38#24594918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20863676-A-C

24594918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20863676-A-G

24595007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 20863769-T-C

24595227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20863985-T-C

24595242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20864000-G-A

24595242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20864000-G-T

24595263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20864021-G-T

24595376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20864196-T-C

24595396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20864218-T-A

24595416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20864242-G-A

http://identifiers.org/hco/10/GRCh38#24595579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20864410-A-C

24595625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20864452-G-C

24595638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20864461-T-A

24596523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20864922-G-T

24596560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20864943-G-C

24596560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20864943-G-T

24596589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20864971-A-G

24596916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20865292-T-A

24597002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20865362-C-T

24597051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20865420-A-G

24597310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20865657-A-T

24597359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20865711-G-A

24597359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20865711-G-T

24598087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20866148-T-C

24598249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20866266-T-C

24598316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20866326-A-G

24598355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20866366-G-A

24598600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20866493-G-A

24600591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20867835-G-A

24600591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20867835-G-C

24600591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20867835-G-T

24600624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20867869-C-T

24600626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20867871-G-A

24600634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20867879-T-C

24600637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20867882-A-G

24600727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20867972-T-C

http://identifiers.org/hco/10/GRCh38#24600739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20867984-C-A

24600739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20867984-C-T

24600754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20867999-C-T

24600781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20868026-A-G

24600934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 20868179-G-C

24600970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20868220-G-A

24601007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20868252-A-G

24601057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20868302-C-G

http://identifiers.org/hco/10/GRCh38#24601059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20868304-C-A

24601084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20868324-A-T

http://identifiers.org/hco/10/GRCh38#24601119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20868678-A-C

24601187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20868745-C-T

24601188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20868746-T-G

24601332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20869510-T-C

24601351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20869536-A-G

24601368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20869552-T-C

24601388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20869572-T-A

24601388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20869572-T-C

24601409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20869588-C-G

24601490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20869632-C-T

24601521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20869666-G-A

24601786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20869933-A-T

24601899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20870006-T-C

24602050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20870148-G-A

24602114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20870213-G-A

24602114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20870213-G-C

24602114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20870213-G-T

24602280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20870391-C-T

24602366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20870526-G-A

24602431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20870587-G-A

http://identifiers.org/hco/10/GRCh38#24602438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20870594-C-A

24602438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20870594-C-T

24602700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20870952-T-C

24602927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20871151-A-T

24603014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20871218-C-T

24603020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20871224-T-C

24603039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20871242-G-A

24603062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20871279-C-G

24603073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20871290-G-A

24603073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20871290-G-C

24603089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20871306-C-T

24603180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20871397-T-C

24603211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20871421-A-G

http://identifiers.org/hco/10/GRCh38#24603374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20871580-C-A

24603451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20871653-T-G

24603538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20871766-G-A

24603540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20871768-G-A

http://identifiers.org/hco/10/GRCh38#24603554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20871782-C-A

24603554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20871782-C-T

http://identifiers.org/hco/10/GRCh38#24603559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20871787-A-C

http://identifiers.org/hco/10/GRCh38#24603612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20871844-A-C

24603621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20871853-G-A

http://identifiers.org/hco/10/GRCh38#24604179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20872432-C-A

24604220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20872470-A-G

24604227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20872473-T-C

24604227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20872473-T-G

24604228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20872474-T-A

24604228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20872474-T-C

24604274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20872517-A-G

24604276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20872519-A-G

http://identifiers.org/hco/10/GRCh38#24604461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20872745-C-A

24604461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20872745-C-T

24604469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20872753-T-C

24605433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20874519-G-A

24605452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20874538-T-C

http://identifiers.org/hco/10/GRCh38#24605476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20874561-A-C

24605566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20874655-T-A

24605566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20874655-T-C

24605606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20874695-A-T

24605653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20874739-A-T

24605908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20874996-A-T

24605964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20875051-T-C

24606051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20875125-G-C

24606097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20875175-G-T

24606116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20875199-T-A

24606857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20875625-A-T

24607004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20875762-A-G

http://identifiers.org/hco/10/GRCh38#24607380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20876089-C-A

24607380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20876089-C-T

24607423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20876129-T-A

24607423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20876129-T-C

http://identifiers.org/hco/10/GRCh38#24607716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20876395-C-A

24607716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20876395-C-T

24607718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20876397-G-A

24607809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20876485-T-A

24607813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20876489-A-G

24607829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20876505-A-G

24607833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20876509-A-G

http://identifiers.org/hco/10/GRCh38#24607869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20876545-A-C

24607870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20876546-A-G

http://identifiers.org/hco/10/GRCh38#24607924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20876597-C-A

http://identifiers.org/hco/10/GRCh38#24608033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20876682-A-C

24608039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20876688-T-A

24608044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20876692-A-T

24608519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20877446-C-T

24608576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20877499-T-A

24608576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20877499-T-C

24608738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20877661-T-C

24608944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20877860-A-G

24608965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20877881-T-C

24608988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20877912-G-A

24617244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20882334-T-G

http://identifiers.org/hco/10/GRCh38#24617302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20882395-C-A

24617302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20882395-C-G

24617310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20882403-T-G

24617535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20882602-G-C

24617537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20882604-G-A

24617537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20882604-G-T

24617546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20882612-T-C

24617550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20882616-T-G

24617571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20882639-G-C

24618340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20883248-T-C

24619489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20884788-A-G

24619564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20884863-T-A

24619978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20885277-G-A

http://identifiers.org/hco/10/GRCh38#24620011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20885310-A-C

24620011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20885310-A-T

24620131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20885430-T-A

24620131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20885430-T-C

24620166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20885465-C-G

24620166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20885465-C-T

24620167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20885466-T-C

24620167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20885466-T-G

24620192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20885491-T-A

24620192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20885491-T-C

24620341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20885637-G-A

24620376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20885672-C-T

24620438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20885734-A-G

24620454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20885750-G-A

24620767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20886063-A-G

24620917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20886213-G-A

24620942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20886235-G-A

24621031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20886324-T-A

24621031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20886324-T-G

24621242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20886535-A-G

http://identifiers.org/hco/10/GRCh38#24621314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20886607-C-A

24621314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20886607-C-G

24621314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20886607-C-T

24621491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20886762-T-C

24621514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20886870-T-C

http://identifiers.org/hco/10/GRCh38#24621516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20886872-C-A

24621516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20886872-C-T

24621570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20886971-T-A

24621799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20887218-T-C

24621814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20887239-A-G

24621844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20887265-A-G

24622321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20887718-A-G

24622321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20887718-A-T

http://identifiers.org/hco/10/GRCh38#24622493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20887826-C-A

24622493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20887826-C-G

24622493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20887826-C-T

24622565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20887886-A-G

http://identifiers.org/hco/10/GRCh38#24622588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20887908-A-C

24622693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20887971-G-T

24622802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20888080-G-A

http://identifiers.org/hco/10/GRCh38#24622953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20888230-A-C

24622953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20888230-A-G

24622962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20888239-T-C

24622962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20888239-T-G

24623030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20888304-A-G

24623069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20888340-C-T

24623088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20888360-G-A

24623158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20888428-G-A

24623617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20888906-G-A

http://identifiers.org/hco/10/GRCh38#24623655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20888942-C-A

24623714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20888988-G-A

24623752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20889026-T-G

24623825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20889085-C-T

24623834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20889094-C-G

24623965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20889199-T-C

24624007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20889233-C-T

http://identifiers.org/hco/10/GRCh38#24624118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20889303-C-A

24624118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20889303-C-T

24624865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20889866-C-T

24625056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20890076-G-A

24625056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20890076-G-C

24625056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20890076-G-T

24625291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20890308-G-A

24625291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20890308-G-C

24625291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20890308-G-T

24625460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20890583-G-A

24625487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20890610-G-A

24625490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20890613-G-A

24625490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20890613-G-T

24626100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20891227-G-A

24626181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20891304-T-C

24629834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20891755-T-C

24629901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20891834-T-G

24630041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20891962-T-C

24630059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20891980-G-A

24630059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20891980-G-T

http://identifiers.org/hco/10/GRCh38#24630087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20892005-A-C

24630184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20892044-T-A

http://identifiers.org/hco/10/GRCh38#24630195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20892055-C-A

24630195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20892055-C-T

24630272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20892122-G-A

24630272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20892122-G-T

http://identifiers.org/hco/10/GRCh38#24630555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20892416-A-C

24630555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20892416-A-G

24630625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20892514-G-A

24630741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20892593-C-T

24631007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20892803-A-G

http://identifiers.org/hco/10/GRCh38#24631384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20892943-A-C

24631402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20892961-T-C

24631587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20893117-A-G

24631648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20893171-T-G

24632522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20893552-T-C

24632796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20894071-G-C

http://identifiers.org/hco/10/GRCh38#24633292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20894595-C-A

24633333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20894624-G-T

24633354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20894647-T-C

http://identifiers.org/hco/10/GRCh38#24633369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20894658-C-A

24633369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20894658-C-T

http://identifiers.org/hco/10/GRCh38#24633526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20894822-C-A

24633526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20894822-C-T

24634117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20895888-T-G

24634573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20896500-G-A

24634573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20896500-G-T

24634660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20896570-T-C

24634757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20896695-C-T

24634862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20896792-T-C

24634967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20896871-G-A

24634967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20896871-G-T

24634968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20896872-A-G

24634976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20896880-A-G

24635213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20897106-A-G

24635213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20897106-A-T

24635244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20897135-T-C

24635287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20897174-T-C

24635431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20897319-G-A

24639262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20897953-G-A

24639320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20898011-G-A

24639320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20898011-G-T

24639339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20898031-T-C

24639580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20898208-G-A

24639632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20898260-C-T

24639932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20898484-C-G

http://identifiers.org/hco/10/GRCh38#24639965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20898505-C-A

24640019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20898553-A-G

24640082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20898616-A-T

24642703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20903234-T-C

24642703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20903234-T-G

24642841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20903516-A-G

24643087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20903699-A-G

http://identifiers.org/hco/10/GRCh38#24643260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20903828-C-A

24643260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20903828-C-T

24645923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20904290-T-C

24645924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20904291-G-A

24646036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20904402-A-G

24646927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20905547-C-T

24647033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20905648-C-T

24647068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20905698-T-C

24647462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20906056-G-A

24647462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20906056-G-C

24647572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20906088-G-A

24661543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20913699-C-T

24661749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20913703-A-G

24661888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20913838-G-A

24661901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20913851-G-A

24662152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20914095-C-T

24662367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20914302-A-T

24662620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20914504-T-C

24664956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20915302-T-A

24665313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20915606-A-T

24665336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20915624-T-C

24665370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20915642-T-C

24665475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20915756-G-A

24665560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20915829-C-T

24665623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20915893-A-G

24665700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20915971-G-C

http://identifiers.org/hco/10/GRCh38#24665823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20916091-A-C

24665996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20916328-T-A

24666238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20916564-G-C

24666738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20916877-T-C

24666806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20916915-G-C

http://identifiers.org/hco/10/GRCh38#24666841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20916949-C-A

24666841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20916949-C-T

24666848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20916958-T-C

24666935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20917038-G-A

24666935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20917038-G-T

24666936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20917039-A-G

24666936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20917039-A-T

24666942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20917045-G-A

24666942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20917045-G-T

24666943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20917046-T-C

24666951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20917052-C-T

24666956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20917057-A-G

24666956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20917057-A-T

http://identifiers.org/hco/10/GRCh38#24667046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20917143-A-C

24667046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20917143-A-G

24667245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20917197-T-C

24667345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20917293-A-G

24667581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20917476-G-A

24667838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20917738-T-C

24668868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20918407-G-A

24668953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20918468-T-C

24669105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20918595-T-C

24669224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20918633-A-T

24669847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20919174-A-G

24670209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20919434-T-C

24670224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20919449-T-A

24670224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20919449-T-C

24670224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20919449-T-G

24670405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 20919630-G-A

24670405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 20919630-G-T

http://identifiers.org/hco/10/GRCh38#24670426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20919650-C-A

24670433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20919657-A-T

http://identifiers.org/hco/10/GRCh38#24670470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20919692-A-C

http://identifiers.org/hco/10/GRCh38#24670481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20919700-A-C

24670481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20919700-A-G

http://identifiers.org/hco/10/GRCh38#24670519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20919767-C-A

http://identifiers.org/hco/10/GRCh38#24670533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20919796-C-A

24670533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20919796-C-T

24670768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20920248-T-A

24670768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20920248-T-G

24670924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20920392-C-G

24670962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20920432-C-G

24671118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20920685-T-C

24671158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20920724-T-C

http://identifiers.org/hco/10/GRCh38#24671200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20920766-C-A

24671200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20920766-C-T

24672618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20924780-C-T

24672769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20924915-T-C

http://identifiers.org/hco/10/GRCh38#24672789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20924935-C-A

24673406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20925616-A-G

http://identifiers.org/hco/10/GRCh38#24673583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20925729-C-A

24673583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20925729-C-T

24673674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20925810-C-T

24680267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20926942-A-T

24680301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20926976-T-C

24680361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20927037-T-C

24680477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20927139-T-C

24680493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20927152-G-T

24680859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20927509-T-C

24681081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20927722-G-A

24681164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20927810-C-T

24681414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20928054-G-A

24681642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20928227-T-A

24681690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20928268-A-G

24681898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20928420-G-A

24681898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20928420-G-C

24681898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20928420-G-T

24682795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20930202-T-A

24682795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20930202-T-C

24682795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20930202-T-G

24684375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20932807-T-C

24685306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20933504-T-A

24687428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20935701-T-A

24687547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20935938-A-G

http://identifiers.org/hco/10/GRCh38#24690972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20939227-C-A

24690973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20939228-A-G

http://identifiers.org/hco/10/GRCh38#24691368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20939760-C-A

24694345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20941308-T-C

24694659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20941617-T-C

24695657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20941944-C-T

24695681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20941968-A-G

24695743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20942030-A-G

24695792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20942084-C-G

24695890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20942344-G-A

24695896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20942359-G-A

24695898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20942361-C-T

24696096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20942575-T-C

24696188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20942651-C-T

24696237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20942701-G-A

24696403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20942868-C-T

24696766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20943260-G-A

24696853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20943336-G-A

24696945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20943402-G-A

24697135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20943538-G-A

24697422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20943729-T-C

24697496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20943767-G-A

24697515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20943786-T-C

24697525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20943796-T-C

24697952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20943902-T-G

24697969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20943920-T-C

24698061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20943999-A-G

24698284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20944180-G-C

24700266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20944658-T-A

24700366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20944772-C-T

24700445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20944854-C-T

http://identifiers.org/hco/10/GRCh38#24703086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20945356-A-C

24703133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20945407-C-T

24703174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20945447-A-T

24703175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20945448-G-A

24703306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20945553-C-T

24703354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20945609-T-C

24703362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20945617-T-C

24703451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20945708-T-C

24703502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20945762-C-T

24703574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20945824-T-C

24703806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20946049-C-T

24703919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20946160-A-G

24703976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20946217-A-G

24705087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20946911-G-A

24705140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20946934-G-C

24705226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20947014-G-A

24705226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20947014-G-T

24705274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20947062-T-A

24705274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20947062-T-C

24705395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20947184-G-C

24705488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20947260-T-C

24705488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20947260-T-G

24706051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20947628-G-A

24706078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20947654-G-T

http://identifiers.org/hco/10/GRCh38#24706130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20947715-C-A

24706131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20947716-A-G

24706203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20947791-C-T

24706211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20947799-T-C

24706262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20947854-C-T

http://identifiers.org/hco/10/GRCh38#24706457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20948045-C-A

24706494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20948082-C-T

24706607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20948189-G-T

http://identifiers.org/hco/10/GRCh38#24706608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#20948190-C-A

24706608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20948190-C-T

24706645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20948217-G-A

24706645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20948217-G-T

24706823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20948362-T-G

24706859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20948396-T-C

24707027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20948552-G-A

24707040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20948561-C-G

24707076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20948597-G-C

24707720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20949212-T-A

http://identifiers.org/hco/10/GRCh38#24707804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20949282-C-A

24707806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20949284-C-G

24707862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20949320-T-C

24707976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20949430-T-C

24713159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20963933-T-C

24713329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20964072-T-C

http://identifiers.org/hco/10/GRCh38#24713416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20964159-C-A

24713612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20964330-T-G

24713820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20964587-T-C

24713952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20964716-T-C

24714053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20965157-A-G

24714158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20965262-G-A

24714158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20965262-G-T

http://identifiers.org/hco/10/GRCh38#24714267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20965377-A-C

24714290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 20965398-A-G

24714417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20965522-G-A

24714652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20965737-C-T

http://identifiers.org/hco/10/GRCh38#24715454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20966169-C-A

http://identifiers.org/hco/10/GRCh38#24715475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20966190-C-A

24715581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20966286-G-A

24715657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20966364-T-C

24716155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20966634-G-C

24716409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20966836-A-G

24716479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20966898-T-C

24716484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20966902-C-T

24716672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20967076-T-C

24716802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20967200-T-A

24717023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20967496-G-C

24717062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20967610-G-A

24717072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20967620-G-A

24717245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20967794-T-C

24718925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20969156-T-C

24718926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20969157-G-T

24718985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20969254-A-G

24719295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20969624-G-C

24719627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20970132-T-C

24719677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20970200-A-G

24720098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20970540-A-G

http://identifiers.org/hco/10/GRCh38#24720234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20970665-C-A

24720412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20970848-C-G

24720971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20971341-A-G

24721044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20971407-A-G

24721105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20971457-T-C

24721227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20971588-G-C

24721371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20971728-C-T

24721404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20971759-G-A

24721405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20971760-T-G

24721668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20972005-G-T

http://identifiers.org/hco/10/GRCh38#24721777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20972096-C-A

24721777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20972096-C-T

http://identifiers.org/hco/10/GRCh38#24721998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20972308-C-A

24722000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20972310-G-A

http://identifiers.org/hco/10/GRCh38#24722388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20972639-A-C

24722712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20972952-G-A

24722748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 20973010-T-C

24722871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20973124-G-T

24722897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20973161-G-A

24722959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20973224-T-C

24722966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20973231-G-C

http://identifiers.org/hco/10/GRCh38#24723315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20973472-A-C

24723315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron variant
orthologous variants: 20973472-A-G

24723371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron_variant, undefined
orthologous variants: 20973513-T-C

http://identifiers.org/hco/10/GRCh38#24723432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20973554-C-A

24723432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron variant
orthologous variants: 20973554-C-G

24723432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: intron variant
orthologous variants: 20973554-C-T

24723574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5 prime UTR variant
orthologous variants: 20973599-G-T

http://identifiers.org/hco/10/GRCh38#24723735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20973615-C-A

24723735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5 prime UTR variant
orthologous variants: 20973615-C-G

24723735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5 prime UTR variant
orthologous variants: 20973615-C-T

http://identifiers.org/hco/10/GRCh38#24723757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#20973637-C-A

24723795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23725
most severe consequence: 5 prime UTR variant
orthologous variants: 20973674-G-C