104310086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47880456-G-T

104310305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47880650-G-A

104310305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47880650-G-T

http://identifiers.org/hco/10/GRCh38#104310306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47880651-C-A

104310321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47880666-T-C

http://identifiers.org/hco/10/GRCh38#104310327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47880672-C-A

104310327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47880672-C-T

104310342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47880686-G-A

104310373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47880706-G-A

104310373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47880706-G-T

http://identifiers.org/hco/10/GRCh38#104310665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47880943-C-A

http://identifiers.org/hco/10/GRCh38#104310682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47880960-C-A

104310682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47880960-C-T

104310762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47881004-T-C

104310963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47881251-G-A

104310963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47881251-G-T

http://identifiers.org/hco/10/GRCh38#104311000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47881347-C-A

104311000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47881347-C-T

104311070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47881403-T-G

http://identifiers.org/hco/10/GRCh38#104311074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47881407-C-A

104311074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47881407-C-T

http://identifiers.org/hco/10/GRCh38#104311193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47881508-C-A

104311193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47881508-C-T

104311207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47881522-T-C

104311218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47881533-T-C

104311305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47881596-T-C

104311437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47881707-A-G

104311453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47881723-A-G

http://identifiers.org/hco/10/GRCh38#104311504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47881763-C-A

http://identifiers.org/hco/10/GRCh38#104311523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47881782-C-A

104311523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47881782-C-T

104311604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47882455-T-C

http://identifiers.org/hco/10/GRCh38#104311605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47882457-C-A

104311608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47882460-C-T

104311661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47882501-T-C

104311683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47882546-G-T

104311701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47882563-G-T

104311757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47882635-G-T

104311787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47882665-C-T

http://identifiers.org/hco/10/GRCh38#104311838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47882708-C-A

http://identifiers.org/hco/10/GRCh38#104311933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47882798-C-A

http://identifiers.org/hco/10/GRCh38#104311956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47882821-C-A

104311956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47882821-C-T

104311987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47882847-G-T

104312012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47882873-T-C

104312013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47882874-G-T

104312036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47882952-G-T

http://identifiers.org/hco/10/GRCh38#104312190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47883085-C-A

104312404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47883287-G-A

104312404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47883287-G-T

104312412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47883295-G-T

http://identifiers.org/hco/10/GRCh38#104312466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47883342-C-A

104312466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47883342-C-T

104312491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47883366-G-T

104312553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47883402-C-T

104312578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47883426-G-T

104312645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47883496-G-A

104312645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47883496-G-T

104312760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47883611-T-C

104312792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47883633-A-G

104312912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47883715-T-C

104313026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47883884-G-A

104313026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47883884-G-T

104313153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47884011-G-T

104313185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47884046-C-T

http://identifiers.org/hco/10/GRCh38#104313191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47884052-C-A

104313191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47884052-C-G

104313191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47884052-C-T

http://identifiers.org/hco/10/GRCh38#104313194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47884055-C-A

http://identifiers.org/hco/10/GRCh38#104313275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47884135-C-A

http://identifiers.org/hco/10/GRCh38#104313302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47885021-C-A

104313302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47885021-C-G

104313302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47885021-C-T

104313400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47884146-T-A

104313400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47884146-T-C

104313402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47884148-T-C

104313594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47884188-T-A

104313594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47884188-T-C

104313594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47884188-T-G

http://identifiers.org/hco/10/GRCh38#104313678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47884269-C-A

104313678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47884269-C-G

104313678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47884269-C-T

104313681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47884272-C-G

104313681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47884272-C-T

http://identifiers.org/hco/10/GRCh38#104313749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47884316-C-A

104313749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47884316-C-G

104313749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47884316-C-T

http://identifiers.org/hco/10/GRCh38#104313771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47884337-C-A

104313771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47884337-C-T

104313782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47884348-T-C

104313810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47884376-T-C

104313894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47884449-G-A

104313894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47884449-G-T

104313965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47884522-C-T

http://identifiers.org/hco/10/GRCh38#104314076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47884623-A-C

104314120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47884668-C-T

104314256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47884806-T-C

104314273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47884823-C-T

104314292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47884843-C-T

104314357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47884903-G-A

104314357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47884903-G-C

104314398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 3 prime UTR variant
orthologous variants: 47884946-G-A

104314561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47885114-G-A

104314561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47885114-G-C

http://identifiers.org/hco/10/GRCh38#104314790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47885343-C-A

104314790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: missense variant
orthologous variants: 47885343-C-G

104314790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: missense variant
orthologous variants: 47885343-C-T

104314834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47885387-G-A

104314852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47885405-G-A

104314942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47885495-A-T

104315017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47885570-G-A

104315212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous_variant, undefined
orthologous variants: 47885765-G-A

104315212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: missense_variant, undefined
orthologous variants: 47885765-G-C

104315225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: missense variant
orthologous variants: 47885790-A-T

104315239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47885804-G-A

104315260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: missense variant
orthologous variants: 47885825-T-G

104315361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: missense variant
orthologous variants: 47885926-G-A

104315476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47886041-G-A

104315476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47886041-G-T

104315503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47886068-G-A

104315511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: missense variant
orthologous variants: 47886076-G-A

104315593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47886158-G-A

104315617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47886182-A-G

104315638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47886203-G-A

104315638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: missense variant
orthologous variants: 47886203-G-C

104315644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47886209-C-G

104315656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47886221-C-T

http://identifiers.org/hco/10/GRCh38#104315683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47886248-C-A

104315695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47886260-C-T

104315707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47886272-G-A

104315740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47886305-C-T

104315743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: stop gained
orthologous variants: 47886308-C-T

104315829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: missense variant
orthologous variants: 47886391-C-T

104315896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47886458-C-T

104315911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47886473-C-T

http://identifiers.org/hco/10/GRCh38#104315980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47886542-C-A

104315980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: synonymous variant
orthologous variants: 47886542-C-T

http://identifiers.org/hco/10/GRCh38#104316060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47886625-C-A

104316060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 47886625-C-T

104316141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47886711-G-T

http://identifiers.org/hco/10/GRCh38#104316174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47886744-C-A

104316174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47886744-C-G

104316174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47886744-C-T

104316204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47886773-G-A

104316210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47886779-G-C

104316249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47886818-C-T

104316306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47886863-C-T

104316424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47886974-G-A

104316443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47886997-G-A

104316443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47886997-G-T

104316646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47887150-C-G

104316646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47887150-C-T

104316648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47887152-C-T

104316703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47887206-A-G

104316718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47887221-C-T

104316719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47887222-C-G

104316719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47887222-C-T

104316748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47887255-C-G

104316835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47887343-T-C

104316927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47887433-G-T

104316969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47887475-G-A

104316978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47887484-A-G

http://identifiers.org/hco/10/GRCh38#104317504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47888763-A-C

104317504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47888763-A-T

104317826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47889070-A-G

104317906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47889133-G-A

104317933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47889161-C-G

104318088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47889305-A-T

104318190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47889411-C-G

104318478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47889637-A-G

104318521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47889684-A-G

104318616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47889780-G-A

104318739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47889839-T-C

http://identifiers.org/hco/10/GRCh38#104318858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47889946-A-C

104319104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47890155-G-C

104319128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47890185-G-T

104319388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47890406-G-A

104319388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47890406-G-T

104319434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47890452-C-T

http://identifiers.org/hco/10/GRCh38#104319561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47890589-C-A

104319640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47890662-A-G

104321121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47890902-C-T

104321539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47891308-C-T

104321544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47891313-C-T

104321640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47891383-C-T

104321734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47891433-T-C

104321750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47891449-G-T

104321835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47891526-G-T

104321862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47891551-C-G

104321862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47891551-C-T

http://identifiers.org/hco/10/GRCh38#104322107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47891740-C-A

104322442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47892020-G-A

104322485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47892051-C-G

104322516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47892082-G-A

104322760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47892342-A-G

104322761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47892343-G-C

104322872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47892460-C-G

104322953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47892529-G-A

http://identifiers.org/hco/10/GRCh38#104323188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47892766-A-C

104323188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47892766-A-G

104323322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47893161-T-C

104323322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47893161-T-G

http://identifiers.org/hco/10/GRCh38#104323424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47893223-C-A

104323424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893223-C-T

http://identifiers.org/hco/10/GRCh38#104323425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47893224-A-C

http://identifiers.org/hco/10/GRCh38#104323430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47893229-C-A

104323448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893247-T-C

104323474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893272-A-G

104323474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893272-A-T

104323524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893330-G-A

http://identifiers.org/hco/10/GRCh38#104323554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47893360-C-A

104323554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893360-C-G

104323554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893360-C-T

104323574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893379-G-A

104323574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893379-G-C

104323606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893411-A-G

104323704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893525-T-C

104323704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893525-T-G

http://identifiers.org/hco/10/GRCh38#104323706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47893527-C-A

http://identifiers.org/hco/10/GRCh38#104323707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47893529-C-A

104323711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893533-G-A

104323711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893533-G-T

104323804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893610-G-A

104323804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893610-G-T

104323850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893617-A-G

104323899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893668-T-C

104323903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893672-G-A

104323903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893672-G-T

http://identifiers.org/hco/10/GRCh38#104323940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47893713-C-A

104323940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 47893713-C-T

104323983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893752-G-A

104323983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893752-G-T

http://identifiers.org/hco/10/GRCh38#104324018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47893785-C-A

104324018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893785-C-T

104324028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893795-G-A

104324028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47893795-G-C

104324269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47894071-C-T

104324277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47894079-G-C

104324277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47894079-G-T

104324315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47894116-T-C

104324449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47894239-T-C

104324726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47894450-T-G

104324792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47894514-C-T

104324874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47894582-A-G

104326078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47896046-C-G

104326101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47896069-T-C

104326101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47896069-T-G

104326194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47896142-T-C

104326275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47896220-G-A

http://identifiers.org/hco/10/GRCh38#104326427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47896334-C-A

http://identifiers.org/hco/10/GRCh38#104326441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47896347-C-A

104326486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47896373-G-T

http://identifiers.org/hco/10/GRCh38#104326601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47896442-C-A

104326637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47896480-T-C

104326641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47896484-T-A

104326641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47896484-T-C

http://identifiers.org/hco/10/GRCh38#104326670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47896514-C-A

104326781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47896598-T-A

104326942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47896733-A-G

104326992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47896750-G-T

http://identifiers.org/hco/10/GRCh38#104327074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47896800-A-C

104327074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47896800-A-G

104327133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47896822-G-A

104327133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47896822-G-T

104327137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47896826-C-T

http://identifiers.org/hco/10/GRCh38#104327143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47896832-C-A

104327143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47896832-C-T

104327379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47897040-C-G

104327379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47897040-C-T

http://identifiers.org/hco/10/GRCh38#104327393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47897051-C-A

104327406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47897064-T-C

104327420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47897065-G-A

104327843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47897460-G-A

104327852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47897469-T-G

104328073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47897696-C-T

http://identifiers.org/hco/10/GRCh38#104328106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47897722-C-A

http://identifiers.org/hco/10/GRCh38#104328123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47897739-C-A

104328123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47897739-C-T

104328159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47897777-G-C

104328204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47897820-C-T

104328243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47897868-C-G

104328243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47897868-C-T

104328339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47897991-A-G

104328711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47898316-T-A

104328838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47898421-A-G

104328902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47898454-G-A

http://identifiers.org/hco/10/GRCh38#104328940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47898480-C-A

104328940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47898480-C-T

http://identifiers.org/hco/10/GRCh38#104328976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47898516-C-A

104328976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47898516-C-T

104329010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47898552-G-A

104329010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47898552-G-C

104329010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47898552-G-T

104329039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47898582-G-A

104329039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47898582-G-T

http://identifiers.org/hco/10/GRCh38#104329040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47898583-C-A

104329040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47898583-C-T

104329041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47898584-A-G

104329042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47898585-T-C

104329052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47898595-C-G

104329052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47898595-C-T

104329054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47898597-C-T

http://identifiers.org/hco/10/GRCh38#104329058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47898601-C-A

104329058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47898601-C-T

104329062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47898605-C-T

104329066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47898609-C-T

104329246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47898835-G-A

http://identifiers.org/hco/10/GRCh38#104329259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47898866-C-A

104329263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47898870-C-T

104329373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47898977-C-T

104329606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47899202-G-A

104329650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47899258-G-C

104329670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47899278-T-C

104329670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47899278-T-G

104329748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47899341-G-A

104329781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47899374-T-G

104329943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47899474-C-T

104329961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47899485-A-T

104329968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47899492-G-A

http://identifiers.org/hco/10/GRCh38#104330058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47899579-C-A

104330058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47899579-C-T

104330059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47899580-T-A

104330106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47899622-T-C

http://identifiers.org/hco/10/GRCh38#104330246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47899740-A-C

104330319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47899811-A-G

104330426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47899912-G-A

104330483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47899953-A-G

104330510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47899983-G-A

104330589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47900059-A-G

http://identifiers.org/hco/10/GRCh38#104330605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47900084-C-A

104330636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47900116-T-C

http://identifiers.org/hco/10/GRCh38#104330689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47900167-C-A

104330780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47900254-T-C

104330923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47900358-G-T

104330937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47900372-T-C

http://identifiers.org/hco/10/GRCh38#104331115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47900488-C-A

104331135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47900507-G-A

104331331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47900697-G-A

104331343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47900709-T-A

104331363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47900729-G-T

104331648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47900982-C-T

104331991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47901477-C-T

104332348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47901892-A-G

104332510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47902052-T-A

104332668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47902222-T-A

104332873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47902454-C-T

104333093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47902631-C-T

104333112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47902649-C-T

104333145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47902681-C-T

104333204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47902732-T-C

104333205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47902733-G-A

104333205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47902733-G-T

http://identifiers.org/hco/10/GRCh38#104333238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47902776-C-A

http://identifiers.org/hco/10/GRCh38#104333275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47902812-C-A

104333303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47902820-G-A

104333303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47902820-G-T

104333490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47903004-G-A

104333490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47903004-G-T

http://identifiers.org/hco/10/GRCh38#104333498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47903012-C-A

104333498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 47903012-C-T

104333543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47903058-A-G

104333543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47903058-A-T

104333553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47903067-C-T

http://identifiers.org/hco/10/GRCh38#104333627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47903139-C-A

104333634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47903146-T-C

104333634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47903146-T-G

104333799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47903267-T-C

104333806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47903274-G-A

104333806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47903274-G-T

http://identifiers.org/hco/10/GRCh38#104333823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47903299-C-A

104333823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47903299-C-T

http://identifiers.org/hco/10/GRCh38#104333941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47903366-C-A

http://identifiers.org/hco/10/GRCh38#104333949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47903374-C-A

104333960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47903385-C-T

104334061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47903468-C-T

104334062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47903469-G-A

104334357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47903758-A-G

104334531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47903911-G-A

104334557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47903939-A-G

104335225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47904765-C-G

104335301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47904842-T-C

104335356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47904897-G-T

104335949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47905389-T-C

104336037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47905461-C-T

104336093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47905494-C-T

http://identifiers.org/hco/10/GRCh38#104336159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47905547-A-C

104336159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47905547-A-T

104336180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47905568-C-T

104336364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47905699-G-A

104336382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47905715-C-T

104336424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47905759-T-G

104337438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47906891-G-A

104337532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47906943-G-A

104337661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47907044-G-A

104337661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47907044-G-C

104337743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47907126-T-C

104337841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47907180-A-G

104338017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47907316-G-A

104338023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron_variant, undefined
orthologous variants: 47907322-A-G

104338032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47907348-G-A

http://identifiers.org/hco/10/GRCh38#104338139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47907437-C-A

104338207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47907512-C-G

104338207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: intron variant
orthologous variants: 47907512-C-T

104338301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5 prime UTR variant
orthologous variants: 47907601-G-T

104338313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5 prime UTR variant
orthologous variants: 47907613-A-G

104338327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5 prime UTR variant
orthologous variants: 47907627-G-A

104338354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5 prime UTR variant
orthologous variants: 47907643-T-C

104338384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47907656-G-A

104338384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47907656-G-T

http://identifiers.org/hco/10/GRCh38#104338399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47907671-C-A

104338399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47907671-C-T

http://identifiers.org/hco/10/GRCh38#104338400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29370
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47907672-C-A