http://identifiers.org/hco/11/GRCh38#34916137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102904228-C-A

34916137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102904228-C-G

34916137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102904228-C-T

http://identifiers.org/hco/11/GRCh38#34916217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102904195-C-A

34916238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, start_lost, undefined
orthologous variants: 102904174-C-T

34916245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 102904167-G-A

34916245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 102904167-G-C

34916245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 102904167-G-T

34916323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 102904116-A-G

http://identifiers.org/hco/11/GRCh38#34916375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#102904067-C-A

34916375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 102904067-C-T

34916385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 102904057-G-A

34916385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 102904057-G-T

34916392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102904050-G-T

34916473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 102903971-T-A

34916473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 102903971-T-C

34916478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 102903966-T-C

34916569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, undefined
orthologous variants: 102903888-T-C

34916594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, undefined
orthologous variants: 102903854-G-A

34916594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, undefined
orthologous variants: 102903854-G-T

34916676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 102903772-G-A

34916676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 102903772-G-C

34916728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 102903720-A-G

34916861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, undefined
orthologous variants: 102903586-G-T

34916874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102903573-G-A

34916874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102903573-G-T

34916891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102903556-G-T

http://identifiers.org/hco/11/GRCh38#34916924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#102903524-C-A

34916924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, undefined
orthologous variants: 102903524-C-T

34917215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, undefined
orthologous variants: 102903230-G-A

34917292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, undefined
orthologous variants: 102903169-A-G

34917355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102903114-G-A

34917422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102903070-T-G

34917549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102902926-G-A

34917599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, undefined
orthologous variants: 102902887-A-G

34918372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102902362-C-T

34918795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102902069-G-A

http://identifiers.org/hco/11/GRCh38#34918963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102901839-C-A

http://identifiers.org/hco/11/GRCh38#34919012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102901791-C-A

34919022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102901783-T-G

34919142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102901681-C-T

34919560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102901325-T-C

34919738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102901169-G-A

34919781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102901139-A-G

34919835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102901086-G-A

34919989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102900921-T-C

34923299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102898792-A-G

34923546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102898532-T-C

http://identifiers.org/hco/11/GRCh38#34924996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102894278-C-A

34925001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102894273-A-G

34925195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102894130-G-T

34926056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102893639-G-A

34926437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102893378-G-A

34926476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102893342-G-A

34926730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102893113-T-C

34926933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102892933-T-C

34926938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, undefined
orthologous variants: 102892928-C-T

34927399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102892506-T-A

34927583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102892366-G-A

34927687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102892263-A-G

34927687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102892263-A-T

34928035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102891933-T-C

34928151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102891827-A-G

34928444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102891551-T-G

34928784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102891295-A-G

34928817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, undefined
orthologous variants: 102891262-C-G

34928983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102891092-T-C

34929021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102891057-G-A

34929079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102891001-T-A

34929531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102890583-G-C

34929767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102890345-G-A

34929813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102890300-T-A

34929963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102890144-T-C

34930099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, undefined
orthologous variants: 102890026-G-A

34930646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102889502-C-T

34930962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102889249-A-T

34931366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102888956-A-G

http://identifiers.org/hco/11/GRCh38#34931382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102888941-C-A

http://identifiers.org/hco/11/GRCh38#34931416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102888908-A-C

34931416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 102888908-A-G

34931448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant
orthologous variants: 102888876-G-A

http://identifiers.org/hco/11/GRCh38#34931509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102888815-C-A

34931509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102888815-C-G

34931509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102888815-C-T

34931518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102888805-T-C

34931558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102888779-T-A

34931558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102888779-T-C

34931608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102888726-T-C

34931608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102888726-T-G

34931734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102888623-A-G

34931769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102888588-A-G

34931857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102888525-G-T

34931898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102888492-A-G

34931982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102888406-G-A

34931982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102888406-G-C

34932137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102888261-T-C

34932203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102888179-C-T

34932360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102887793-C-T

34932511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102887667-G-A

34932866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102887421-T-G

34932885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102887402-C-T

34933343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102886962-T-C

34933493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102886820-T-C

34933565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102886745-T-A

34933583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102886728-C-T

34933738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102886592-T-C

34933981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102886368-T-C

34934037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102886316-T-C

34934037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102886316-T-G

34934244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102886088-T-C

34934299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102886037-C-G

34934301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102886035-A-G

34935068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102885667-C-G

34935068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102885667-C-T

34935183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102885561-T-A

34935957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102884768-A-G

34938237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102884200-A-G

34938268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102884179-T-A

34938384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102884090-C-G

http://identifiers.org/hco/11/GRCh38#34938386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102884088-A-C

34938429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102884045-A-G

34939458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102883786-T-G

34939471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102883773-G-A

34939550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102883726-A-T

34939896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102883432-C-T

34939981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102883357-T-C

34939996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102883342-G-A

34939996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102883342-G-C

34940197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102883230-A-G

34940197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102883230-A-T

34940216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102883215-G-A

34940216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102883215-G-T

http://identifiers.org/hco/11/GRCh38#34940241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102883194-C-A

34940367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102883061-G-A

34940507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102882921-C-T

34940571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102882865-T-C

http://identifiers.org/hco/11/GRCh38#34940585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102882851-A-C

34940585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102882851-A-G

34940609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102882827-G-T

34940691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102882773-C-T

34941584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102882563-A-T

34941726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102882450-G-T

34941738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102882443-G-A

34941738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102882443-G-T

34941771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102882428-A-G

34941785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102882414-T-C

34941785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102882414-T-G

34941824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102882375-A-G

34941855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 102882344-G-A

34941855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 102882344-G-T

34941856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 102882343-A-G

34941883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102882328-G-C

34941883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102882328-G-T

http://identifiers.org/hco/11/GRCh38#34941891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#102882320-C-A

34941896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 102882315-G-T

http://identifiers.org/hco/11/GRCh38#34941907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#102882304-C-A

34941907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 102882304-C-G

34941907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 102882304-C-T

34942048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102882177-C-T

34942376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102881986-T-C

34942954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102881561-A-G

34943242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102881313-A-G

34943255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102881300-T-C

34943385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102881186-C-G

34943386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102881185-T-C

34943500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102881082-G-A

34943523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102881059-G-A

34943669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102880955-G-A

34943680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102880945-C-G

34943680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102880945-C-T

34943860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102880815-A-G

34943997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102880699-T-A

34944040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102880656-A-G

34944475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102880620-G-A

http://identifiers.org/hco/11/GRCh38#34944507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102880580-C-A

34944881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102880215-C-T

34945302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102879888-G-A

34945503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102879699-A-G

34945798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102879442-T-C

34945996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102879265-A-G

34945997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102879264-G-C

34946027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102879235-A-G

34946294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102879050-A-T

34946914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102878054-G-A

http://identifiers.org/hco/11/GRCh38#34946953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102878018-C-A

34947015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102877957-C-T

34947096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102877887-A-G

34947113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102877870-T-C

34947124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102877859-T-C

http://identifiers.org/hco/11/GRCh38#34947173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102877760-C-A

34947231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102877646-T-G

34947243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102877634-A-G

34947295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102877591-T-C

34947467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102877209-T-C

34947529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: missense variant
orthologous variants: 102877141-G-A

http://identifiers.org/hco/11/GRCh38#34947717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102876997-C-A

34947742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102876973-A-G

34947976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102876761-G-A

34947976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102876761-G-T

34948063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102876675-T-C

34948382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102876413-G-A

34948382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102876413-G-T

34948444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102876338-G-A

34948599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102876161-T-C

34948730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102876038-G-A

34948995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102875785-T-G

34949107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102875681-A-G

34949112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102875676-G-A

34949114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102875674-A-G

34949137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102875651-A-G

34954931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102874649-G-C

34955047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102874572-C-T

34956258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102874156-C-T

34956951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102873485-A-G

34957044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102873399-C-T

34957241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102872857-G-T

34957245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102872853-G-T

http://identifiers.org/hco/11/GRCh38#34957474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102872646-A-C

34957474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant
orthologous variants: 102872646-A-G

34957513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant
orthologous variants: 102872607-G-A

34957607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102872513-A-G

34957607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102872513-A-T

34957794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102872370-C-G

34957983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102872201-A-G

34960330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102871574-T-A

http://identifiers.org/hco/11/GRCh38#34960378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102871527-A-C

34960378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102871527-A-G

34960378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102871527-A-T

http://identifiers.org/hco/11/GRCh38#34960442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102871462-C-A

34960442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant
orthologous variants: 102871462-C-G

34960442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant
orthologous variants: 102871462-C-T

http://identifiers.org/hco/11/GRCh38#34960544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102871355-C-A

34962233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102869786-A-G

34962871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102869171-A-T

34963092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102868992-T-C

34963533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102868867-G-A

34963877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102868558-A-G

34964017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102868422-C-G

34964017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102868422-C-T

http://identifiers.org/hco/11/GRCh38#34966470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102865872-C-A

34966555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102865817-T-A

http://identifiers.org/hco/11/GRCh38#34966711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102865661-C-A

34966711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant
orthologous variants: 102865661-C-T

34966774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant
orthologous variants: 102865598-T-A

34966774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant
orthologous variants: 102865598-T-C

34966775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 102865597-G-C

34966822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 102865550-T-A

34966839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102865532-A-T

34968329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102864365-G-C

34968625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102864136-T-G

34969767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102864003-T-C

34969997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102863799-T-C

34970067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102863746-A-T

34970104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102863709-T-A

34970127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102863667-G-A

34970127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102863667-G-C

34970134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 102863660-T-A

34970134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 102863660-T-C

34970155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant
orthologous variants: 102863637-T-C

34970388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102863421-T-A

34970925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102863039-T-C

34971288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102862613-T-C

34971315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102862584-T-C

34971367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102862564-G-A

34971418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102862510-G-A

34971594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102862362-T-G

34971741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102862157-T-C

34977819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, undefined
orthologous variants: 102861082-T-C

34977835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron variant
orthologous variants: 102861067-C-T

34977860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, undefined
orthologous variants: 102861042-G-T

34977957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102860854-G-A

34977957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102860854-G-T

http://identifiers.org/hco/11/GRCh38#34977958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102860853-C-A

34977958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102860853-C-T

34978112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102860691-T-C

34978188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102860615-T-A

34978188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102860615-T-C

34978246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102860568-A-G

34978335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102860515-A-G

34978346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102860504-C-G

34979935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102860270-A-G

34980110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102860134-A-G

34980110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102860134-A-T

34980202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102860047-A-T

http://identifiers.org/hco/11/GRCh38#34980219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102860030-A-C

34980477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102859879-G-A

34980742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102859511-A-G

34980877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102859359-G-T

34980909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102859327-T-C

34984436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102858902-T-C

34984461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102858877-T-C

34984757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102858593-A-G

http://identifiers.org/hco/11/GRCh38#34984786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102858568-C-A

34984786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102858568-C-G

34984948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102858431-T-G

34984981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102858392-C-T

34985524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102857835-T-A

34985599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102857760-G-A

34985610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102857749-T-G

34985619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102857740-T-C

34985655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102857707-T-C

34986541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102856980-G-C

34986658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102856880-T-C

34986672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102856866-A-G

34987897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102856640-C-G

34988014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102856549-A-G

34988017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102856546-A-G

34988184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102856321-G-A

34988246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102856173-A-G

34988318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102856071-C-G

34988563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102855842-A-G

34989427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102855626-T-A

34989476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102855579-T-C

34989643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102855450-A-T

34989681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102855413-A-G

34989723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102855371-A-G

34992171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102854706-T-C

34992175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102854702-G-C

34992221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102854663-G-T

34992224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102854660-A-G

http://identifiers.org/hco/11/GRCh38#34992242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102854642-C-A

http://identifiers.org/hco/11/GRCh38#34992291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102854592-C-A

34992291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102854592-C-G

34992291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102854592-C-T

34992380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 102854507-G-A

http://identifiers.org/hco/11/GRCh38#34992442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102854463-C-A

http://identifiers.org/hco/11/GRCh38#34992447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102854458-C-A

34992447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102854458-C-T

http://identifiers.org/hco/11/GRCh38#34992486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102854408-C-A

34992509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102854385-T-A

34992509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102854385-T-C

34992522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102854372-A-G

34992727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102854149-C-G

34992789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102854087-C-T

34992866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102854022-A-G

34992866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102854022-A-T

34992994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102853890-C-T

34993273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102853623-T-A

34993370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102853532-G-T

34993447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102853463-C-T

34993591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102853349-G-A

34993603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102853337-C-T

34994719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102852896-T-C

http://identifiers.org/hco/11/GRCh38#34994795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102852826-C-A

34994795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102852826-C-T

34994819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102852796-A-T

http://identifiers.org/hco/11/GRCh38#34994825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102852790-C-A

34994873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102852655-T-G

34994879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102852649-C-T

34994951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102852575-A-G

http://identifiers.org/hco/11/GRCh38#34995020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102852506-A-C

34995020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102852506-A-G

34995061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 102852465-G-A

34995068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102852458-A-G

34995107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102852419-G-A

34995107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102852419-G-C

34995277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102852307-G-T

34995281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102852303-T-C

34995297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102852287-G-A

34995297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102852287-G-T

34995323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102852262-T-G

34995669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102851939-T-C

34995669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102851939-T-G

34995672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102851936-T-C

34995672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102851936-T-G

http://identifiers.org/hco/11/GRCh38#34995683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102851924-A-C

34995683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102851924-A-G

34995683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102851924-A-T

http://identifiers.org/hco/11/GRCh38#34995697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102851917-C-A

34995805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102851815-A-G

34995915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102851573-G-A

http://identifiers.org/hco/11/GRCh38#34996257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102851251-A-C

34996573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102850942-T-C

34997097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102850502-C-T

34997710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102849986-A-T

34997787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102849891-C-G

34997890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102849794-A-G

34998291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102849424-C-G

34998553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102849178-C-G

34999053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102848529-A-G

34999192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102848409-T-G

34999431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102848016-T-A

34999431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102848016-T-C

34999571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102847882-C-T

34999710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102847768-G-A

35000146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102846899-C-G

35001084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102845239-C-T

35001266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102845104-T-C

35001740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102843882-T-A

35001806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102843829-T-C

35001806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102843829-T-G

35001817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102843818-G-A

35001829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102843802-T-C

35001830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102843801-T-C

35001971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102843654-A-G

35002878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102843196-C-G

35002878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102843196-C-T

35003007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102843095-T-G

35003008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102843094-C-T

35003015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102843087-G-C

35003137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102842991-G-A

35003191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102842933-C-T

35003251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102842775-G-A

35003472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102842482-T-C

http://identifiers.org/hco/11/GRCh38#35003541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102842265-C-A

http://identifiers.org/hco/11/GRCh38#35003734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102842126-A-C

35004112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102841737-G-C

35005503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102840031-C-G

35005794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102839803-A-G

35005794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102839803-A-T

35005796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102839801-A-T

35005824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102839783-T-C

35005857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102839747-A-T

35005994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102839645-T-G

35006039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102839602-C-T

35006143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102839513-T-A

35006176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102839481-C-T

35006317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102839361-T-C

35006744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102838865-C-T

35007098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102838529-C-G

35007143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102838484-C-G

35007466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102837722-C-T

http://identifiers.org/hco/11/GRCh38#35007779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102837382-C-A

35007877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102837246-A-G

35007877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102837246-A-T

35008688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102836088-C-T

35008796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102835976-A-G

35009333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102835409-T-C

35009467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102835280-T-C

35009571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102835178-T-C

35009571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102835178-T-G

35009574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102835175-C-T

35009703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102835086-A-G

35009933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102834846-A-T

35009949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102834830-G-A

35010032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102834575-A-G

35010110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102834498-T-C

35011238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102832567-T-A

35011318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102832405-C-T

35011362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102832362-C-T

35011438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102832283-C-G

35011561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102832169-T-C

35011840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102831419-C-T

35011845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102831414-G-A

35011864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102831395-G-A

http://identifiers.org/hco/11/GRCh38#35011953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102831261-C-A

35011953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102831261-C-G

35011972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102831240-G-A

35012014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102831194-G-A

35012014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102831194-G-T

35012255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102830525-A-G

35012450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102830042-C-T

35012748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102829870-G-A

35013404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102829576-T-G

35013716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102829272-G-A

35014145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102828841-G-A

http://identifiers.org/hco/11/GRCh38#35014640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102828312-A-C

http://identifiers.org/hco/11/GRCh38#35014815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102828144-C-A

35014823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102828136-A-G

35015259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102827817-A-G

35017275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102825311-G-A

35017351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102825253-A-G

35017351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102825253-A-T