30202631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148807135-G-A

http://identifiers.org/hco/13/GRCh38#30202674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148807177-C-A

30202674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148807177-C-T

30202848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148807332-C-T

30202885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148807369-T-C

30202922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148807389-T-C

http://identifiers.org/hco/13/GRCh38#30203038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148807454-C-A

30203056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148807471-C-T

30203106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148807526-T-C

30203592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148808305-T-C

30203593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148808306-G-A

30204030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148808721-C-G

30204030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148808721-C-T

http://identifiers.org/hco/13/GRCh38#30204144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148808881-C-A

30204165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148808900-G-T

30204201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148808940-T-C

http://identifiers.org/hco/13/GRCh38#30204204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148808943-A-C

30204268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148809000-C-T

30204272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148809004-A-T

30204421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148809180-A-T

30204667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148809394-T-C

30204707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148809424-G-T

30204760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148809467-A-G

http://identifiers.org/hco/13/GRCh38#30204819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148809515-C-A

30204819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148809515-C-T

30204901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148809608-G-A

30204901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148809608-G-T

30205012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148809712-G-T

30205084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148809803-G-A

30205151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148809918-T-C

http://identifiers.org/hco/13/GRCh38#30205251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148810023-A-C

30205277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148810045-G-A

30205277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148810045-G-C

30205277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148810045-G-T

http://identifiers.org/hco/13/GRCh38#30206978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148811611-C-A

30206978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148811611-C-G

30206999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148811632-A-G

30207066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148811692-G-A

30207116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148811738-G-C

30207189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148811782-T-C

30207200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148811793-A-G

30207260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148811866-G-A

30207303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148811903-G-A

30207636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812161-G-A

30207636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812161-G-T

30207643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812168-T-C

30207643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812168-T-G

http://identifiers.org/hco/13/GRCh38#30207867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148812405-C-A

30207927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812445-G-A

30207927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812445-G-C

http://identifiers.org/hco/13/GRCh38#30207953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148812470-A-C

30207953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812470-A-G

30208152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812636-A-T

http://identifiers.org/hco/13/GRCh38#30208155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148812639-C-A

30208155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812639-C-T

30208190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812642-T-A

30208198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812650-A-G

30208221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812679-G-T

http://identifiers.org/hco/13/GRCh38#30208265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148812698-C-A

30208281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812710-T-C

30208282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812711-G-T

30208299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812728-G-A

http://identifiers.org/hco/13/GRCh38#30208317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148812740-A-C

30208317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812740-A-T

http://identifiers.org/hco/13/GRCh38#30208338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148812761-A-C

http://identifiers.org/hco/13/GRCh38#30208368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148812780-C-A

30208378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812790-T-C

30208413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812828-G-C

30208413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812828-G-T

http://identifiers.org/hco/13/GRCh38#30208441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148812853-C-A

30208457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812870-T-A

30208466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812879-G-A

30208466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812879-G-C

30208466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812879-G-T

30208488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812899-T-C

30208488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 3 prime UTR variant
orthologous variants: 148812899-T-G

30208543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: synonymous variant
orthologous variants: 148812951-A-G

30208618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: synonymous variant
orthologous variants: 148813026-T-C

30208618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: synonymous variant
orthologous variants: 148813026-T-G

http://identifiers.org/hco/13/GRCh38#30208754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148813161-A-C

30208754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148813161-A-G

30208799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148813205-T-C

30208799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148813205-T-G

30208849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148813284-T-C

30208849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148813284-T-G

30208939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148814230-A-G

30208965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148814254-G-A

30209305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148814522-T-C

30209316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148814533-G-A

30209396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148814608-G-A

30209409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148814621-T-C

30209447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148814679-T-C

30209526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148814755-C-T

http://identifiers.org/hco/13/GRCh38#30209539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148814768-A-C

30209605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148814822-T-C

30209605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148814822-T-G

30209644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148814853-T-C

30210133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148815516-T-C

30210133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148815516-T-G

30210134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148815517-T-C

http://identifiers.org/hco/13/GRCh38#30210269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148815632-C-A

30210269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148815632-C-T

30210327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148815679-A-G

30210429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148815781-A-G

30210464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148815814-G-A

30210467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148815817-G-A

30210474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148815825-G-T

http://identifiers.org/hco/13/GRCh38#30210537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148815874-C-A

http://identifiers.org/hco/13/GRCh38#30210558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148815895-A-C

30210558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148815895-A-G

30210685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148815978-T-A

30210685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148815978-T-G

30210695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148815988-T-A

30210740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148816031-T-C

30210778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148816065-G-A

30210778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148816065-G-T

30211643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148817103-C-T

30211730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148817151-T-C

30211882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148817285-A-G

http://identifiers.org/hco/13/GRCh38#30212061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148817412-A-C

30212146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148817502-T-C

30221028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148820287-A-G

30221310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148820564-G-A

30221310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148820564-G-C

http://identifiers.org/hco/13/GRCh38#30226080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148824555-C-A

30226114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148824587-T-C

30226150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148824622-T-C

30226198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148824683-T-G

30226539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148824992-T-C

30226753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148825198-G-A

30226944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148825478-T-C

30227250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148825619-G-C

30227250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148825619-G-T

http://identifiers.org/hco/13/GRCh38#30227292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148825624-C-A

30227292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148825624-C-T

30227342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148825629-A-G

30227347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148825634-G-T

30227382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148825671-A-G

30227382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148825671-A-T

30227479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: synonymous variant
orthologous variants: 148825756-G-A

30227582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148825861-C-G

30227662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148825933-C-T

30227676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148825950-G-C

30227676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148825950-G-T

30227688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148825962-G-A

30227688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148825962-G-T

30227719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148825988-A-G

30227815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148826024-T-C

30227972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148826192-G-A

30228526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148826663-T-A

30228666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148826798-T-C

30229094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148827279-T-C

30229206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148827390-C-G

30229243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148827427-G-A

30229875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148827894-G-A

30230048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148828063-C-T

30230057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148828072-T-C

30230110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148828126-G-A

30230165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148828174-T-G

30230310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148828282-C-G

30230314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148828286-A-G

30230353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148828323-G-A

30230353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148828323-G-T

30230371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148828335-T-C

30230526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: synonymous variant
orthologous variants: 148828497-G-C

30230537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: stop gained
orthologous variants: 148828508-G-A

30230537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: synonymous variant
orthologous variants: 148828508-G-T

30230641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148828612-A-G

30230650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148828621-A-T

30231029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148829079-T-C

30231112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148829121-T-C

http://identifiers.org/hco/13/GRCh38#30231181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148829181-C-A

30231181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148829181-C-T

http://identifiers.org/hco/13/GRCh38#30231193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148829193-A-C

30231301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148829303-T-C

30231386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: synonymous variant
orthologous variants: 148829392-G-A

30231389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: missense variant
orthologous variants: 148829395-G-C

30231572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148829579-A-G

http://identifiers.org/hco/13/GRCh38#30231581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148829589-C-A

30231581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148829589-C-T

30231588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148829596-G-A

30231588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148829596-G-T

30240151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148830205-C-T

http://identifiers.org/hco/13/GRCh38#30240290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148830339-A-C

http://identifiers.org/hco/13/GRCh38#30240340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148830386-C-A

30240340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148830386-C-T

http://identifiers.org/hco/13/GRCh38#30240346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148830392-C-A

30240346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148830392-C-G

30240348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148830400-T-C

http://identifiers.org/hco/13/GRCh38#30240390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148830433-C-A

30240390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148830433-C-G

30240390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148830433-C-T

http://identifiers.org/hco/13/GRCh38#30240424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148830460-C-A

30240424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148830460-C-G

30240424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148830460-C-T

30240577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148830610-C-T

30240594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148830619-G-T

30240599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148830624-C-G

30240758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148830789-G-C

30241091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 148831091-G-A

30241112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148831110-A-G

30241124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148831122-T-C

30241170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148831296-C-T

30241238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148831382-C-G

30241238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148831382-C-T

30241307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148831452-G-C

30241389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148831500-G-A

30241689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148832494-A-G

30241790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148832565-A-G

30241837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148832609-C-T

30241954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148832723-T-C

30241989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148832751-T-C

30242172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148832931-A-G

http://identifiers.org/hco/13/GRCh38#30242203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148832961-A-C

30242298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148833035-G-A

30242552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148833251-T-C

30242737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148833407-T-C

30242896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148833464-A-G

30242962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148833528-T-A

30243064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148833645-T-A

http://identifiers.org/hco/13/GRCh38#30243170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148833747-C-A

30243170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148833747-C-T

30243435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148834020-C-G

30243602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148834157-T-A

http://identifiers.org/hco/13/GRCh38#30243609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148834164-A-C

30243661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148834196-T-A

30243695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148834226-T-C

30243797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148834287-C-T

30247005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148834885-A-G

30247199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148835022-T-C

http://identifiers.org/hco/13/GRCh38#30247283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148835102-A-C

30247364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148835185-C-T

30248010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148835422-A-G

30248347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148835698-T-C

30248506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148835795-G-C

30248517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148835804-A-G

http://identifiers.org/hco/13/GRCh38#30250487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148838157-A-C

http://identifiers.org/hco/13/GRCh38#30250575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148838237-A-C

30250602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148838265-C-T

30250640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148838300-G-A

30251377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148838876-T-C

30251397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148838896-T-C

30251667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148839165-T-C

30251876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148839312-G-T

30252088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148839514-T-A

30252103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148839529-T-C

30252187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148839643-A-G

http://identifiers.org/hco/13/GRCh38#30252226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148839682-C-A

30252320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148839755-C-G

30252502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148839950-C-T

30252853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148840251-T-C

30252853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148840251-T-G

30255246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148841234-A-G

30255253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148841241-T-C

30255312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148841300-T-A

30255312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148841300-T-C

30255327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148841314-G-T

30255387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148841330-T-A

30255387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148841330-T-C

30255411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148841351-T-C

30255465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 148841395-T-C

30255585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 148841509-T-A

30255585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 148841509-T-C

30255609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 148841533-T-A

30255609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 148841533-T-C

30255609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 148841533-T-G

http://identifiers.org/hco/13/GRCh38#30255656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148841585-A-C

30255656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148841585-A-G

30255667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148841600-G-A

30255667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148841600-G-T

http://identifiers.org/hco/13/GRCh38#30255669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148841602-C-A

30255669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148841602-C-T

30255831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148841809-C-G

30255905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148841868-T-G

30255980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148841924-T-C

30256104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148842023-A-T

30256153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148842072-T-A

30256310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148842226-T-C

30256482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148842363-C-G

30257837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148845133-C-T

http://identifiers.org/hco/13/GRCh38#30257849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148845145-A-C

30258139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148845418-G-A

30273511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148847721-G-A

30273751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148847919-A-G

30276372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148852442-G-A

30276466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148852540-T-C

30276479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148852553-T-C

http://identifiers.org/hco/13/GRCh38#30276517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148852565-A-C

30276586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148852594-T-C

30276602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148852609-C-G

30276622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148852625-T-A

30277030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148852803-A-G

30277318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148853037-T-C

30277349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148853075-A-G

30277709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148853401-C-T

30277725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148853417-T-G

30277738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148853430-C-T

30277768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148853477-G-C

30277792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148853504-G-A

http://identifiers.org/hco/13/GRCh38#30277797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148853509-A-C

30277810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148853520-C-T

30277811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148853521-G-A

30278242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148853947-G-A

30278389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148854160-C-G

30278534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148854299-T-C

30279220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148854902-A-G

30279401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148855051-G-A

30279675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148855093-T-G

30280249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148855587-G-A

30280249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148855587-G-T

30280259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148855597-G-A

30280259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148855597-G-C

30280259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148855597-G-T

30280324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148855663-G-A

30280324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148855663-G-T

http://identifiers.org/hco/13/GRCh38#30280337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148855676-A-C

30280337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148855676-A-G

30280337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148855676-A-T

30280620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148855835-A-G

30280645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148855853-C-T

30280729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148855933-A-G

30280860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148856016-A-G

30281210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148856147-A-T

http://identifiers.org/hco/13/GRCh38#30281260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148856181-A-C

30281260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148856181-A-G

30281336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148856255-T-G

30281346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148856265-T-C

30281625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148856483-A-G

30281631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148856489-T-C

http://identifiers.org/hco/13/GRCh38#30281642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148856500-C-A

30283510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148857944-G-A

30283510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148857944-G-T

30283800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148858228-A-G

30283805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148858234-A-G

30284531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148858764-G-A

30284980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148859245-C-T

30285025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148859289-G-C

30285043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148859305-G-A

30306630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: 148865097-G-C

30306737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148865198-C-G

30306757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 148865218-T-C

30306823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148865266-T-C

30306864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148865271-G-A

30306864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148865271-G-T

30306878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148865282-G-T

30306905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148865308-G-A

30306905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148865308-G-T

30306911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148865310-A-G

30307010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148865406-A-G

30307058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, undefined
orthologous variants: 148865452-G-A

30307058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, undefined
orthologous variants: 148865452-G-T

30307117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, undefined
orthologous variants: 148865510-G-C

30307129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, undefined
orthologous variants: 148865522-T-G

http://identifiers.org/hco/13/GRCh38#30307164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#148865555-C-A

http://identifiers.org/hco/13/GRCh38#30307192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#148865589-C-A

30307192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, undefined
orthologous variants: 148865589-C-T

30307200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, undefined
orthologous variants: 148865597-A-G

http://identifiers.org/hco/13/GRCh38#30307229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#148865608-C-A

http://identifiers.org/hco/13/GRCh38#30307247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#148865624-C-A

30307247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, undefined
orthologous variants: 148865624-C-T

http://identifiers.org/hco/13/GRCh38#30307284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#148865656-C-A

http://identifiers.org/hco/13/GRCh38#30307302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#148865669-C-A

http://identifiers.org/hco/13/GRCh38#30307400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#148865762-C-A

30307400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 148865762-C-T

30307452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 148865808-G-A

30307452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28361
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 148865808-G-T