20136160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119432713-C-T

20136674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119432243-T-C

20136713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119432185-C-T

20136743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119432155-A-G

20137112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119432037-G-C

20137112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119432037-G-T

20137258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119431940-G-T

20137271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119431927-G-A

20137341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119431867-T-C

20137460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119431757-A-G

20137490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119431728-C-T

http://identifiers.org/hco/7/GRCh38#20137548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119431683-C-A

20137632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119431599-A-G

20137749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119431482-A-T

20137805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119431427-A-G

20137805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119431427-A-T

http://identifiers.org/hco/7/GRCh38#20138317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119431160-C-A

20138334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119431143-T-C

20138525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119430916-G-C

20138641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119430811-C-T

20138654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119430798-A-G

http://identifiers.org/hco/7/GRCh38#20138987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119430765-C-A

20138987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119430765-C-T

20139257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119430494-G-T

20139543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119430228-A-G

20139677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119430104-G-T

20139788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119430002-T-C

20139961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119429892-G-T

20140108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119429758-A-G

20140305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119429595-C-G

20140305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119429595-C-T

20140332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119429564-T-C

20140332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119429564-T-G

20140920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3 prime UTR variant
orthologous variants: 119429427-T-A

20140920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 3 prime UTR variant
orthologous variants: 119429427-T-C

20141121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: stop gained
orthologous variants: 119429230-C-T

http://identifiers.org/hco/7/GRCh38#20141443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119428906-A-C

20141740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, undefined
orthologous variants: 119428421-A-G

20141921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119428243-T-C

20142330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119427883-T-G

20142354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119427858-C-T

20142572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119427551-G-A

20142672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119427321-T-C

20143052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119426795-A-T

20143411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119426532-C-T

http://identifiers.org/hco/7/GRCh38#20143839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119426391-C-A

20143839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119426391-C-T

20143868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119426362-G-A

20143951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119426280-T-C

20144019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119426237-A-G

http://identifiers.org/hco/7/GRCh38#20144123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119426140-A-C

20145266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119424821-G-A

20145288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119424799-T-C

20145359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119424727-G-A

20145359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119424727-G-C

20145631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119424530-T-C

20145634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119424527-G-A

20146304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119423824-G-A

20146621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119423538-A-G

20146705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119422750-A-G

20146927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119422183-G-A

http://identifiers.org/hco/7/GRCh38#20146947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119422092-C-A

20147322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119421740-T-A

20147322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119421740-T-C

20147335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119421727-A-G

20147480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119421580-G-A

20147480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119421580-G-C

20147480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119421580-G-T

20147579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119421496-T-C

20147579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119421496-T-G

20147834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119421064-T-C

20147844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119421054-T-C

20147951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119420949-T-C

20148041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119420869-C-G

20148420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119420490-G-A

20148544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119420370-T-G

http://identifiers.org/hco/7/GRCh38#20148859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119420075-A-C

20148900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119420034-C-G

20149010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119419941-A-T

http://identifiers.org/hco/7/GRCh38#20149047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119419902-A-C

20149544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119419434-G-C

20149574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119419405-G-A

20149721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119419301-G-A

20149904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119419131-C-T

20149908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119419127-G-A

20150175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119418868-T-C

20150230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119418833-G-A

http://identifiers.org/hco/7/GRCh38#20150290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119418769-A-C

20151246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119417761-G-A

20151333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119417682-T-A

20151764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119416758-A-T

20151931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119416298-T-C

20152456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119415838-C-T

20152888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119415426-G-C

http://identifiers.org/hco/7/GRCh38#20152958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119415356-C-A

20153125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119415200-T-A

20153125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119415200-T-C

20153219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119415122-G-A

20153656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119414663-G-T

20153767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119414559-G-C

20153837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119414493-T-C

20153842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119414488-T-C

20154130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119414228-A-G

20154269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: stop gained
orthologous variants: 119414090-A-T

http://identifiers.org/hco/7/GRCh38#20154638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119413725-C-A

20155000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119413468-C-T

20155581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119413263-T-A

20155623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119413221-A-G

20156280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119412720-G-A

20156340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119412665-G-A

20157338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119411925-C-T

20157433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119411838-G-A

20157518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119411785-T-C

20157575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119411769-G-A

20157575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119411769-G-C

20157584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119411760-G-A

http://identifiers.org/hco/7/GRCh38#20158060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119411516-A-C

20158060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119411516-A-G

20158226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: missense variant
orthologous variants: 119411363-T-C

20158226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: missense variant
orthologous variants: 119411363-T-G

20158802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: missense variant
orthologous variants: 119410790-T-A

20158802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: missense variant
orthologous variants: 119410790-T-C

http://identifiers.org/hco/7/GRCh38#20159034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119410558-C-A

20159288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: missense variant
orthologous variants: 119410304-G-A

20159288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: missense variant
orthologous variants: 119410304-G-T

20159810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: missense variant
orthologous variants: 119409782-C-G

20159810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: missense variant
orthologous variants: 119409782-C-T

http://identifiers.org/hco/7/GRCh38#20159837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119409755-C-A

20159837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: missense variant
orthologous variants: 119409755-C-T

http://identifiers.org/hco/7/GRCh38#20159957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119409635-C-A

20160090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: missense variant
orthologous variants: 119409502-T-C

20160434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119409160-T-C

20160683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119408926-G-C

20161393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119408296-C-T

20161432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119408253-G-C

20161814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: missense variant
orthologous variants: 119407191-T-C

20161921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: 119407084-G-T

http://identifiers.org/hco/7/GRCh38#20161984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119407025-C-A

20164910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119404478-G-A

20164910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119404478-G-T

20164978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119404408-G-T

20165019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119404367-T-A

20165164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119404179-C-T

http://identifiers.org/hco/7/GRCh38#20165352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119404009-C-A

20165509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119403878-T-C

20165791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119403615-T-C

20165975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119403438-G-T

20166312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119396845-C-G

20166379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119396776-T-C

20166557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119396644-A-G

20166563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119396634-G-A

20168135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119395610-G-A

20168135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119395610-G-T

http://identifiers.org/hco/7/GRCh38#20168237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119395526-C-A

20168463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119395337-C-T

20168709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119395103-C-T

20168740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119395073-G-T

http://identifiers.org/hco/7/GRCh38#20168746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119395067-A-C

http://identifiers.org/hco/7/GRCh38#20168803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119395007-C-A

20168803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119395007-C-G

20168973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119394226-G-A

20169188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119394087-T-A

20169188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119394087-T-C

http://identifiers.org/hco/7/GRCh38#20169568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119393722-A-C

20169642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119393645-T-C

20169860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119393445-G-A

20170087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119393121-G-A

20170087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119393121-G-T

http://identifiers.org/hco/7/GRCh38#20170101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119393107-C-A

20170117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119393085-G-T

20170384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119392850-G-A

20170575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119391215-G-A

20170575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119391215-G-T

20170592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119391199-T-C

20170634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119391156-G-A

20170688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119391111-C-G

20170694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119391099-G-T

20172630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119390994-T-C

20172950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119390718-G-A

20172985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119390683-G-T

20172988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119390680-C-G

http://identifiers.org/hco/7/GRCh38#20173044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119390631-C-A

http://identifiers.org/hco/7/GRCh38#20173101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119390577-C-A

20173101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119390577-C-G

20173124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119390545-G-A

20173124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119390545-G-T

http://identifiers.org/hco/7/GRCh38#20173233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119390415-C-A

20173718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119390103-A-G

20173788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119390050-C-T

20174136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119389732-T-C

20174185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119389683-G-A

20174216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119389640-A-G

20174453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119389404-T-C

20174656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119388959-T-C

20177728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119385172-T-C

20177765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119385137-A-T

20177768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119385134-G-C

20177768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119385134-G-T

20177854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119385036-A-G

20178050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119384847-C-T

20178206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119384713-T-C

20184967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119381696-A-T

20185021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119381637-A-G

20185042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119381618-C-T

20185057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119381603-C-T

20185471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119381202-A-G

20185527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119381149-A-T

20185550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119381135-C-G

20185642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119381044-G-A

20185891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119380817-C-G

20185939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119380770-C-T

20185961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119380748-C-T

http://identifiers.org/hco/7/GRCh38#20186274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119380486-A-C

http://identifiers.org/hco/7/GRCh38#20186461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119380283-C-A

20186726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119380016-G-A

20190511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119378246-T-C

20190675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119378081-C-T

20190725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119378031-C-T

http://identifiers.org/hco/7/GRCh38#20190965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119377818-A-C

20191139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119377645-G-C

20191303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119377472-T-G

20191365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119377429-G-C

20191379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119377414-G-A

20191585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119377263-C-T

http://identifiers.org/hco/7/GRCh38#20191834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119377053-C-A

20191834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119377053-C-T

20191837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119377050-C-T

20191905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119376982-A-G

20191964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119376932-T-A

http://identifiers.org/hco/7/GRCh38#20191997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119376879-A-C

20192099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119376636-T-C

20192100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119376635-T-G

20192468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119376036-G-A

20192468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119376036-G-C

20192645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119375875-G-A

20192700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119375820-T-C

20192882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119375651-A-G

20193089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119375464-A-G

20193880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119374679-C-T

http://identifiers.org/hco/7/GRCh38#20193929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119374615-A-C

20193970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119374573-G-C

20194328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119374105-C-T

http://identifiers.org/hco/7/GRCh38#20196710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119370755-C-A

20196710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119370755-C-T

20197142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119370351-A-G

20197581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119369599-C-T

20197627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119369553-T-C

http://identifiers.org/hco/7/GRCh38#20197709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119369469-A-C

20197717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119369461-C-T

20197805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119369375-C-T

20197920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119369249-A-G

20198045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119369137-G-T

20198119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119369076-G-A

20198460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119368733-G-T

20198468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119368725-G-C

20198468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119368725-G-T

20198517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119368677-A-T

http://identifiers.org/hco/7/GRCh38#20198588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119368605-C-A

http://identifiers.org/hco/7/GRCh38#20198618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119368590-C-A

20199083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119367912-A-G

20199205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119367808-C-T

20199359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119367666-A-G

20199385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119367639-T-C

20199481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119367551-T-C

20199481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119367551-T-G

20199638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119367389-A-G

20200447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119366837-T-C

20200551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119366733-T-C

20200820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119366466-A-T

http://identifiers.org/hco/7/GRCh38#20203416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119364922-A-C

20203748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119364618-T-C

20203751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119364615-G-A

20203751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119364615-G-C

20203776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119364592-G-C

20203854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119364513-T-G

20203867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119364487-A-G

20204155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119364175-T-C

20204551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119363827-C-T

20204744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119363649-T-C

http://identifiers.org/hco/7/GRCh38#20205226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119363190-A-C

http://identifiers.org/hco/7/GRCh38#20205332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119363099-C-A

20205599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119362941-C-G

20205599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119362941-C-T

20205828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119362724-T-C

http://identifiers.org/hco/7/GRCh38#20205936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119362626-C-A

20206061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119362529-G-A

http://identifiers.org/hco/7/GRCh38#20206099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119362491-C-A

20206099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119362491-C-T

20206101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119362488-C-T

20206148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119362441-G-C

20206680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119362001-C-T

20210403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119360283-T-C

http://identifiers.org/hco/7/GRCh38#20210627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119360086-C-A

20210627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119360086-C-T

20210661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119360052-C-T

20210707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119360002-G-A

20211344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119359291-T-C

20211449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119359226-A-G

20211740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119358925-G-A

20211751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119358914-T-C

20211995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119358683-T-C

http://identifiers.org/hco/7/GRCh38#20212430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119357885-A-C

20212569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119357737-G-T

20212570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119357736-T-G

20212581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119357725-T-C

http://identifiers.org/hco/7/GRCh38#20212660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119357657-C-A

20212660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119357657-C-T

20214149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119357070-A-G

20214178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119357017-G-C

20214280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119356922-T-A

20214285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119356917-T-A

20214399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119356824-C-T

20214430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119356800-T-C

http://identifiers.org/hco/7/GRCh38#20214642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119356600-C-A

20214642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119356600-C-T

20214666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119356576-G-A

20214674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119356568-T-C

20214760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119356495-C-T

20214879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119356382-T-C

20215361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119355975-T-C

20215396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119355940-T-C

20215396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119355940-T-G

20215917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119355687-T-C

http://identifiers.org/hco/7/GRCh38#20216035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119355573-A-C

20216088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119355518-A-G

http://identifiers.org/hco/7/GRCh38#20216198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119355405-A-C

20216231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119355372-A-G

20216242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119355361-G-C

20216252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119355353-A-G

http://identifiers.org/hco/7/GRCh38#20216454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#119355201-A-C

20216908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119354847-T-C

20217134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119354641-T-C

20217139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119354636-C-G

http://identifiers.org/hco/7/GRCh38#20217239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#119354532-C-A

20217239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119354532-C-T

20217254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30215
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119354517-T-C