http://identifiers.org/hco/6/GRCh38#41033640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48768091-C-A

41033640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48768091-C-G

41033651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48768080-A-G

41033651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48768080-A-T

41033657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48768074-A-G

41033657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48768074-A-T

41033693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48768040-T-C

41033725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48768005-A-G

41033725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48768005-A-T

41033745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48767985-A-G

41033775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48767955-A-G

41033775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48767955-A-T

41033790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48767917-A-G

http://identifiers.org/hco/6/GRCh38#41033801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48767906-A-C

41033801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48767906-A-G

41033845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48767847-T-G

41033944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48767748-G-A

http://identifiers.org/hco/6/GRCh38#41033992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48767700-C-A

41033992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48767700-C-T

41034100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48767592-G-A

http://identifiers.org/hco/6/GRCh38#41034279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48767421-C-A

41034279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48767421-C-T

http://identifiers.org/hco/6/GRCh38#41034292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48767414-C-A

41034292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48767414-C-G

41034292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48767414-C-T

41034332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48767377-G-C

41034610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48767086-G-A

41034610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48767086-G-T

41034615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48767081-T-C

41034700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 48767000-G-A

41034700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 48767000-G-C

41034741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48766959-C-T

41034904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 48766796-G-A

41034968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48766732-G-A

http://identifiers.org/hco/6/GRCh38#41035132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48766568-A-C

41036920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48765044-C-G

41036920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48765044-C-T

41036965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48765009-C-T

41037064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48764936-C-T

41037247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48764815-G-A

41037337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48764725-T-C

41037433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48764634-T-C

41037457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48764624-C-T

41037644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48764447-A-G

http://identifiers.org/hco/6/GRCh38#41038272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48763341-C-A

41038496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48763079-G-A

41038629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48762947-A-G

41038938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48762208-G-T

41039008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48762137-T-C

http://identifiers.org/hco/6/GRCh38#41039074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48762068-C-A

41039074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48762068-C-T

http://identifiers.org/hco/6/GRCh38#41039078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48762062-C-A

41039078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48762062-C-T

41039079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48762061-C-T

41039110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48762043-C-T

http://identifiers.org/hco/6/GRCh38#41039121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48762032-C-A

http://identifiers.org/hco/6/GRCh38#41039132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48762022-C-A

41039132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48762022-C-T

41039147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48762008-G-A

41039147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48762008-G-T

http://identifiers.org/hco/6/GRCh38#41039189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48761971-C-A

41039189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48761971-C-T

41039257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48761893-A-G

http://identifiers.org/hco/6/GRCh38#41039273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#48761877-C-A

41039273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48761877-C-T

41039310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48761840-G-A

41039310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48761840-G-C

http://identifiers.org/hco/6/GRCh38#41039312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48761838-C-A

http://identifiers.org/hco/6/GRCh38#41039315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48761835-C-A

41039321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48761829-G-C

41039447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48761686-G-A

41039643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48761525-T-C

http://identifiers.org/hco/6/GRCh38#41041104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48758882-C-A

41041184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48758696-C-T

41041587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48758327-G-A

41042150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48758176-T-C

41042151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48758175-G-A

41042155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48758171-A-G

41042216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48758088-G-T

41042241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48758064-G-A

http://identifiers.org/hco/6/GRCh38#41042427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48757888-A-C

41042427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48757888-A-G

http://identifiers.org/hco/6/GRCh38#41042502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48757817-C-A

41042502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48757817-C-T

41042531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48757788-T-C

41042531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48757788-T-G

41042550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48757759-G-A

41042550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48757759-G-T

41042554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48757742-A-G

41042554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48757742-A-T

41042628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48757446-T-A

41042628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48757446-T-C

41042631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48757443-T-C

http://identifiers.org/hco/6/GRCh38#41042716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48757315-C-A

41042716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48757315-C-T

http://identifiers.org/hco/6/GRCh38#41042743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48757298-A-C

41042816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 48757231-A-T

http://identifiers.org/hco/6/GRCh38#41042849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48757201-C-A

41042976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48757086-T-C

41043022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48757042-C-G

41043022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48757042-C-T

http://identifiers.org/hco/6/GRCh38#41043136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48756931-A-C

41043163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48756904-G-C

41043167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48756900-T-C

41043170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48756874-T-C

41043217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48756801-T-C

http://identifiers.org/hco/6/GRCh38#41043408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48756299-A-C

41043408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48756299-A-G

http://identifiers.org/hco/6/GRCh38#41043452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48756255-C-A

http://identifiers.org/hco/6/GRCh38#41043502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48756235-C-A

41043502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48756235-C-T

http://identifiers.org/hco/6/GRCh38#41043585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48756159-C-A

41043599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48756145-G-C

http://identifiers.org/hco/6/GRCh38#41043686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48756058-C-A

http://identifiers.org/hco/6/GRCh38#41043748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48756003-C-A

41043748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48756003-C-T

http://identifiers.org/hco/6/GRCh38#41043780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48755984-A-C

41043890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755882-G-A

41043890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755882-G-T

41043924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755845-C-T

41044287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48755504-G-C

41044287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48755504-G-T

http://identifiers.org/hco/6/GRCh38#41044303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48755490-C-A

41044356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755442-T-A

41044442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755378-T-A

41044442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755378-T-C

41044442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755378-T-G

41044475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755348-C-G

41044510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755316-C-T

41044525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755301-C-T

41044618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755094-G-A

41044671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755027-G-A

41044671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755027-G-T

41044746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48754967-T-C

41045067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48754592-C-T

41045142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48754522-A-T

41045150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48754514-T-C

41045293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48754373-C-T

41045317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48754349-G-A

41045441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48754219-C-T

41047821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48745555-G-C

http://identifiers.org/hco/6/GRCh38#41047893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48745472-A-C

41047995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48745364-A-T

41047997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48745362-C-T

http://identifiers.org/hco/6/GRCh38#41048206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48745144-C-A

41048431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48744910-C-T

http://identifiers.org/hco/6/GRCh38#41048450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48744891-A-C

41048450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48744891-A-G

41048481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48744860-C-T

41048550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48744789-C-G

41048833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48744506-C-T

41048889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48744461-G-A

41048940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48744412-G-A

41048940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48744412-G-C

http://identifiers.org/hco/6/GRCh38#41049213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48744162-A-C

41050003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48743434-A-G

41050009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48743419-C-T

41050121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48743316-T-C

41050126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48743311-A-G

41050297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48743149-G-A

http://identifiers.org/hco/6/GRCh38#41050310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48743138-C-A

41050660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48742464-C-T

41050908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48742226-C-T

41051367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48742074-C-T

41051412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48742015-C-T

41051684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48741586-C-T

41051704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48741566-T-C

41051724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48741528-T-C

41051742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48741505-G-A

41051795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48741395-T-C

http://identifiers.org/hco/6/GRCh38#41052832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48740057-C-A

http://identifiers.org/hco/6/GRCh38#41052892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48739998-A-C

41052968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48739975-G-A

http://identifiers.org/hco/6/GRCh38#41053208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48739751-C-A

41053225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48739743-T-C

http://identifiers.org/hco/6/GRCh38#41053236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48739732-C-A

41053236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48739732-C-T

http://identifiers.org/hco/6/GRCh38#41053342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48739641-C-A

41053438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 48739545-A-T

41053498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48739485-C-T

41053520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48739465-G-A

http://identifiers.org/hco/6/GRCh38#41053523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48739462-C-A

41053523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48739462-C-T

41053610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48739396-T-A

41053635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48739372-C-T

41054145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48738831-G-C

41054181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48738797-G-A

41054220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48738761-G-A

41054249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48738732-T-C

41054392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48738619-G-A

41054431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48738586-G-C

41054521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48738502-G-C

41054776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48738238-G-A

http://identifiers.org/hco/6/GRCh38#41054797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48738217-C-A

41055171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48737800-A-G

41055541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48737504-G-A

41055541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48737504-G-T

41056008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48737007-G-C

41056463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48736653-A-G

41056619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48736489-T-G

41056632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48736476-T-C

41056671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48736438-T-C

41056747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48736379-G-T

41056784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48736342-T-C

41056891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48736236-G-A

41056918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48736214-C-T

41057059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48736143-G-C

41057070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48736132-T-C

http://identifiers.org/hco/6/GRCh38#41057135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48736071-A-C

41058315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48734642-T-A

http://identifiers.org/hco/6/GRCh38#41058358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48734596-C-A

http://identifiers.org/hco/6/GRCh38#41058390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48734581-A-C

41058414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48734557-C-T

41058493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48734502-T-C

http://identifiers.org/hco/6/GRCh38#41058531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48734465-A-C

41058891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48734161-C-T

41058958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48734098-G-A

41058964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48734091-A-G

41058964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48734091-A-T

41059045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48734012-G-C

41059173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48733866-C-T

41059453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48733522-G-T

41059481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48733506-G-A

41059487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48733500-G-A

41059509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48733478-G-A

41059527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48733462-C-T

41059603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48733387-T-C

41059885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48733129-A-G

41059910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48733103-C-T

http://identifiers.org/hco/6/GRCh38#41060212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48732165-C-A

41060522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48731510-G-C

41060663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48731385-C-T

http://identifiers.org/hco/6/GRCh38#41060954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48731175-A-C

41060954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48731175-A-T

41061184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48730802-T-A

41061184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48730802-T-C

41061184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48730802-T-G

41061271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48730591-G-A

41061271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48730591-G-C

41061437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48730422-G-T

41061476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48730383-C-T

41061516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48730343-T-C

http://identifiers.org/hco/6/GRCh38#41061548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48730311-A-C

41061620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48730239-A-T

41061641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48730218-A-T

41061913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48729946-G-C

http://identifiers.org/hco/6/GRCh38#41062506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48729069-C-A

41062795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48728784-T-A

41063251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48728331-A-G

41063279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48728326-C-T

41063326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48728283-G-T

41063391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48728220-G-C

41064028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48726706-C-T

41064050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48726702-C-T

41064061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48726691-G-A

http://identifiers.org/hco/6/GRCh38#41064172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48726592-C-A

41064192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48726575-T-C

41064231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48726532-A-T

41064233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48726530-T-C

41064287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48726478-G-T

41064469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48726300-T-C

41064642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48726118-A-G

http://identifiers.org/hco/6/GRCh38#41064663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48726096-C-A

41064664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48726095-A-G

41064684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48725693-G-C

41064684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48725693-G-T

41064728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48725656-G-A

41064728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48725656-G-T

41064760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48725621-C-T

41064912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48725494-T-C

http://identifiers.org/hco/6/GRCh38#41064940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48725477-C-A

41065068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48725346-A-G

41065148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48725287-C-T

41065490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48725057-C-T

http://identifiers.org/hco/6/GRCh38#41065492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48725055-C-A

41065492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48725055-C-T

41065514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48725033-T-C

http://identifiers.org/hco/6/GRCh38#41065575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48724990-A-C

41065575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48724990-A-G

41065769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48724867-T-C

41065774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48724862-G-A

41065774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48724862-G-T

http://identifiers.org/hco/6/GRCh38#41065784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48724853-C-A

41065784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48724853-C-T

http://identifiers.org/hco/6/GRCh38#41065830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48724811-C-A

41065830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48724811-C-T

http://identifiers.org/hco/6/GRCh38#41065877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#48724767-C-A

41065877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48724767-C-G

41065923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48724722-G-A

41065941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48724704-G-A

41065941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48724704-G-T

41066014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48724636-G-A

41066052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48724589-A-G

41066655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48724416-T-G

http://identifiers.org/hco/6/GRCh38#41066734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48724338-C-A

41066734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48724338-C-T

41066799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48724274-C-T

http://identifiers.org/hco/6/GRCh38#41066948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#48724155-C-A

41066948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48724155-C-T

41067080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48724021-A-G

41067227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48723919-A-T

41067261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48723887-G-A

41067261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48723887-G-T

http://identifiers.org/hco/6/GRCh38#41067276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48723869-C-A

41067276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48723869-C-T

http://identifiers.org/hco/6/GRCh38#41067473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48723627-A-C

41067473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48723627-A-G

41067476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48723624-G-C

41067476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48723624-G-T

41067544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48723562-T-A

41067544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48723562-T-C

41067553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48723555-T-C

http://identifiers.org/hco/6/GRCh38#41067563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48723545-C-A

41067563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48723545-C-G

41067875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48723281-G-C

41067887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48723269-G-A

http://identifiers.org/hco/6/GRCh38#41067992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48723186-A-C

41068014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48723180-C-T

41068082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48723110-T-G

41068249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48722810-G-A

41068392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48722700-T-A

41068456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48722637-G-A

41068502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48722593-T-C

41068585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48722524-T-C

41068693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48722416-T-G

41068827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48722373-A-G

41068827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48722373-A-T

41068862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48722338-A-T

41069003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48722183-A-T

41069088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48722088-T-C

http://identifiers.org/hco/6/GRCh38#41069132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48722069-A-C

41069136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48722065-C-T

http://identifiers.org/hco/6/GRCh38#41069142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48722063-A-C

41069142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48722063-A-G

41069144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48722061-A-T

41069150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48722055-T-A

41069150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48722055-T-C

http://identifiers.org/hco/6/GRCh38#41069168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48722039-C-A

41069168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48722039-C-T

41069175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48722032-G-A

41069215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48722008-A-G

http://identifiers.org/hco/6/GRCh38#41069224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48721999-A-C

41069224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48721999-A-G

41069306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48721947-A-G

41069306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48721947-A-T

http://identifiers.org/hco/6/GRCh38#41069412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48721848-C-A

41069441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48721827-A-G

41069478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48721791-C-T

41069551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48721721-A-G

http://identifiers.org/hco/6/GRCh38#41069554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48721720-C-A

41069600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48721688-C-T

41069625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48721664-G-A

41069625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48721664-G-T

41069903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48721453-A-G

41069939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48721417-G-A

41070037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48721327-A-G

41070037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48721327-A-T

http://identifiers.org/hco/6/GRCh38#41070714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48719481-C-A

41070770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48719427-G-A

41070770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48719427-G-C

41070770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48719427-G-T

41070793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48719410-T-C

http://identifiers.org/hco/6/GRCh38#41070794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48719409-C-A

41070794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48719409-C-T

http://identifiers.org/hco/6/GRCh38#41070937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48718669-A-C

41070937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48718669-A-T

41070970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48718636-G-C

41070970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48718636-G-T

41070983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48718623-T-C

41070983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48718623-T-G

41071073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 48718497-T-C

41071349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48718233-T-C

http://identifiers.org/hco/6/GRCh38#41071409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48718157-C-A

41071421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48718123-G-T

41071482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48718056-A-G

41071482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48718056-A-T

http://identifiers.org/hco/6/GRCh38#41071515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48718012-A-C

41071515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48718012-A-T

41072071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48717570-G-C

41072112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48717555-G-A

41072142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48717541-G-A

41072142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48717541-G-T

41072183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48717504-G-A

41072183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48717504-G-T

41072194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48717493-A-G

41072269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48717441-T-C

http://identifiers.org/hco/6/GRCh38#41072325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#48717408-C-A

41072325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 48717408-C-T

41072529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48717199-G-T

41072596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 48717132-G-A

41072596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 48717132-G-T

41072624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, undefined
orthologous variants: 48717103-G-A

41072624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, undefined
orthologous variants: 48717103-G-T

41072654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, undefined
orthologous variants: 48717072-G-A

41072654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, undefined
orthologous variants: 48717072-G-T

41072661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, undefined
orthologous variants: 48717064-T-C

41072702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48717030-A-G

http://identifiers.org/hco/6/GRCh38#41072762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48716971-C-A

41072850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48716884-G-T

41072852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48716882-G-A

41072878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48716856-T-G

41072904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48716832-G-A

41072985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 48716751-G-A

41072985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 48716751-G-C

41072985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 48716751-G-T

41072997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 48716739-G-A

41072997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 48716739-G-T

41073006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 48716730-G-A

41073006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 48716730-G-T

http://identifiers.org/hco/6/GRCh38#41073215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48716522-C-A

41073215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48716522-C-T

41073358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, undefined
orthologous variants: 48716409-A-T

41073370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, undefined
orthologous variants: 48716397-G-A

41073459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, undefined
orthologous variants: 48716340-G-A

41073459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, undefined
orthologous variants: 48716340-G-T

41073550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, undefined
orthologous variants: 48716264-C-T

41074364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48715644-C-T

41074773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48715324-T-G

41075378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48715232-T-A

41075385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48715225-A-G

http://identifiers.org/hco/6/GRCh38#41075454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48715159-C-A

41075548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 48715079-A-G

http://identifiers.org/hco/6/GRCh38#41075641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48715016-C-A

41075641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 48715016-C-T

http://identifiers.org/hco/6/GRCh38#41075643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48715014-C-A

41075643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 48715014-C-T

41076990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48714269-A-T

41077001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48714258-G-A

41077173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48714080-G-T

41077493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48713813-A-G

41077570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48713742-T-C

41078896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48707757-A-G

41079132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, missense_variant
orthologous variants: 48707496-A-G

41079172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 48707456-A-G

41079879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48706833-G-A

41080334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48706532-A-G

41080452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48706412-C-T

41080531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron variant
orthologous variants: 48706337-T-G

http://identifiers.org/hco/6/GRCh38#41080718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48706181-C-A

41080718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48706181-C-T

41080732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48706167-A-G

41080995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48705919-G-T

41081944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48705327-A-G

41082437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48704764-G-A

41082507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48704701-G-A

41082507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48704701-G-T

41082711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48704389-A-G

41083026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48703931-C-T

http://identifiers.org/hco/6/GRCh38#41083088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48703868-A-C

41083207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48703761-A-G

41083908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48702953-T-C

41083988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48702877-G-T

41084160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 48702708-G-A

41084197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48702671-G-A

41087198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48702180-A-G

41087224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48702155-T-C

41087572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48701894-G-T

http://identifiers.org/hco/6/GRCh38#41089551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48700606-A-C

41089594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 48700563-C-G

41090176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48700334-G-A

41090176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48700334-G-T

http://identifiers.org/hco/6/GRCh38#41090319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48700197-C-A

41090319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48700197-C-T

41090335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48700183-G-A

41090335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48700183-G-C

41090341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48700177-T-C

http://identifiers.org/hco/6/GRCh38#41090375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48700143-C-A

41090380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48700136-T-C

41090380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48700136-T-G

41090415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48700113-T-A

41090437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48700091-T-A

41090437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48700091-T-G

http://identifiers.org/hco/6/GRCh38#41090449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48700079-C-A

41090456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48700072-G-T

41091385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48699692-G-A

41091435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48699651-G-A

41091435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48699651-G-T

41091713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48699341-C-T

41091721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48699335-T-C

41091813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48699229-G-A

41091813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48699229-G-T

41093087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 48698900-T-C

41093152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48698849-T-A

41093413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48698674-C-T

41094106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48698486-T-C

41094338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48698429-A-G

41094339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48698428-T-C

http://identifiers.org/hco/6/GRCh38#41094347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48698422-C-A

41097372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 48696353-G-A

41097422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48696304-G-A

41097429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48696297-A-T

41097751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48695988-G-A

41097751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48695988-G-C

41097751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21257
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48695988-G-T