174283841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 5 prime UTR variant
orthologous variants: 57003976-C-T

174283845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 5 prime UTR variant
orthologous variants: 57003967-G-T

174283847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 5 prime UTR variant
orthologous variants: 57003965-G-A

174283867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 57003946-T-C

http://identifiers.org/hco/4/GRCh38#174283890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57003923-C-A

174283890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 5 prime UTR variant
orthologous variants: 57003923-C-T

174284155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 57003662-G-T

http://identifiers.org/hco/4/GRCh38#174284189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57003628-C-A

174284189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57003628-C-T

174284252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57003565-A-G

174284441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57003397-C-G

174284441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57003397-C-T

174284465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57003374-C-G

174284819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57003066-T-C

174285268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57002568-G-C

174285374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57002472-A-G

174285375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57002471-T-C

174285425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57002426-G-A

174285426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 57002425-T-C

http://identifiers.org/hco/4/GRCh38#174285554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57002278-A-C

http://identifiers.org/hco/4/GRCh38#174285637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57002208-A-C

174285732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57002181-A-G

174285968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57001953-A-T

174286264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57001712-T-G

174286411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57001566-G-T

174298847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57000799-A-T

174298951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57000685-G-A

174298951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57000685-G-T

174299011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57000614-G-A

174299011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57000614-G-T

http://identifiers.org/hco/4/GRCh38#174299030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57000594-A-C

174299054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57000573-A-G

174299089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 57000538-T-G

174299107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 57000520-A-G

174299140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 57000491-A-T

174299149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 57000482-T-G

174299173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 57000458-C-T

174299179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 57000452-C-T

174299188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 57000443-C-G

174299215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57000416-G-A

http://identifiers.org/hco/4/GRCh38#174299406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56999807-C-A

174301150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56999358-T-A

http://identifiers.org/hco/4/GRCh38#174301155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56999353-A-C

174301332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56999178-A-G

174301481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56999084-C-G

174301521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56999049-G-A

174301521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56999049-G-C

http://identifiers.org/hco/4/GRCh38#174301605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56998988-C-A

174301666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56998929-A-G

174301709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56998888-G-A

174301709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56998888-G-T

174301768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56998841-G-A

http://identifiers.org/hco/4/GRCh38#174301921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56998684-C-A

174301921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56998684-C-G

174301921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56998684-C-T

174301946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56998662-A-G

174302100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 56998524-T-C

174302106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 56998518-T-C

174302116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 56998508-A-T

174302157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 56998467-G-T

174302214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56998410-A-G

174302224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56998403-G-A

174302224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56998403-G-T

174302270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56998249-A-G

http://identifiers.org/hco/4/GRCh38#174302273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56998246-C-A

http://identifiers.org/hco/4/GRCh38#174302282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56998052-C-A

174302282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56998052-C-T

174302298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56998036-T-C

174302349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56997985-A-G

174302504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56997854-C-T

174302527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56997832-G-T

174303588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56997399-G-T

http://identifiers.org/hco/4/GRCh38#174303668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56997327-C-A

174303668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56997327-C-T

http://identifiers.org/hco/4/GRCh38#174303715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56997285-C-A

174303715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 56997285-C-T

174303758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 56997242-A-G

174303779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 56997221-A-G

http://identifiers.org/hco/4/GRCh38#174303899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56997106-C-A

http://identifiers.org/hco/4/GRCh38#174303901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56997104-C-A

174303901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56997104-C-T

174303933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56997085-A-G

http://identifiers.org/hco/4/GRCh38#174303950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56997068-A-C

174303950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56997068-A-G

174303950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56997068-A-T

174303953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56997065-G-T

174303962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56996493-G-A

174303962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56996493-G-T

http://identifiers.org/hco/4/GRCh38#174304155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56996158-C-A

174304155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56996158-C-T

174304156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56996157-A-G

174304215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56996095-T-C

174304247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 56996061-A-G

174304247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 56996061-A-T

174304301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 56996007-G-A

174304392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56995915-T-C

174304396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56995911-A-G

174304397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56995910-T-C

174304397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56995910-T-G

174304407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56995900-G-A

174304512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56995718-T-C

174304939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56995163-C-G

174304939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56995163-C-T

174304956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56995146-T-C

174304991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56995106-C-T

174305037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56995071-A-G

174305102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56995007-G-C

http://identifiers.org/hco/4/GRCh38#174308751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56994004-A-C

174308751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 56994004-A-G

174308751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 56994004-A-T

174308788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 56993970-G-A

174308788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 56993970-G-T

174308832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56993926-G-A

174308833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56993925-G-A

174308833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56993925-G-T

http://identifiers.org/hco/4/GRCh38#174308836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56993922-C-A

http://identifiers.org/hco/4/GRCh38#174308934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56993839-C-A

174308934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56993839-C-T

174308939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56993834-G-T

174308941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56993832-A-G

174308997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56993791-G-T

174309146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56993643-G-T

174309162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56993627-G-A

174309650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56993102-G-A

http://identifiers.org/hco/4/GRCh38#174309706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56993044-C-A

174309874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56992911-A-T

174309982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56992803-G-A

174310027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56992758-C-G

174310104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56992699-T-C

174310104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56992699-T-G

174310497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56992330-A-G

174310560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56991929-T-C

http://identifiers.org/hco/4/GRCh38#174310595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56991886-A-C

174310595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56991886-A-G

174310755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56991743-T-C

174310837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56991665-G-A

174310840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56991662-A-G

174310935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56991555-T-A

174310935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56991555-T-C

174310994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56991136-G-T

174311650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56990618-C-T

http://identifiers.org/hco/4/GRCh38#174311671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56990597-C-A

174311695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56990574-T-C

174311751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56990502-G-A

174311751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56990502-G-T

174311762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56990491-A-G

http://identifiers.org/hco/4/GRCh38#174311777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56990477-A-C

174311818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56990436-T-G

174312158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56990149-G-A

174312623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56990076-C-T

174312762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56989957-C-T

174312936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56989784-G-A

174313080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56989676-T-C

174313080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56989676-T-G

174313106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56989642-T-C

174313127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56989619-A-G

http://identifiers.org/hco/4/GRCh38#174313254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56989508-A-C

174313312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56989453-C-T

174313387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56989391-A-G

174314208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56988696-A-G

174314270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56988637-C-T

174314460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56988460-C-G

http://identifiers.org/hco/4/GRCh38#174314475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56988444-C-A

174314475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56988444-C-T

174314485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56988434-C-G

174314616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56988130-C-G

174314616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56988130-C-T

174314660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56988085-G-C

174314715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56988027-T-C

174314975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56987787-T-C

174314982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56987780-T-A

174314982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56987780-T-C

174314986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56987776-C-T

http://identifiers.org/hco/4/GRCh38#174315028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#56987738-A-C

174315028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56987738-A-G

174315045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56987721-A-G

174315095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56987683-G-A

174315095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56987683-G-C

174315264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56987553-C-T

174315354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56987464-A-G

174315496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56986644-T-C

174316152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56985947-T-G

174316180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56985919-G-A

174316180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56985919-G-C

http://identifiers.org/hco/4/GRCh38#174316189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56985910-C-A

174316340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56985756-G-A

174316340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56985756-G-C

http://identifiers.org/hco/4/GRCh38#174316435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56985642-C-A

174316518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56985559-T-C

174316617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56985463-T-C

http://identifiers.org/hco/4/GRCh38#174316626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56985454-A-C

174316630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56985450-T-A

174316630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56985450-T-C

174316648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56985432-G-C

http://identifiers.org/hco/4/GRCh38#174316726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56985360-C-A

174316726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56985360-C-T

174316739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56985314-G-A

174316739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56985314-G-T

174317194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56984890-G-A

174317194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56984890-G-T

http://identifiers.org/hco/4/GRCh38#174317250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56984839-C-A

174317250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56984839-C-G

http://identifiers.org/hco/4/GRCh38#174317272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56984828-C-A

174317272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56984828-C-G

174317287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56984813-T-C

174317297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56984803-T-C

http://identifiers.org/hco/4/GRCh38#174317377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/8/GRCm39#56984723-C-A

174317377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 56984723-C-G

174317377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 56984723-C-T

174317379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 56984721-T-C

174317383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_retained_variant
orthologous variants: 56984717-G-A

174317383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 56984717-G-T

174317395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56984705-T-C

174317396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56984704-G-A

174317396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56984704-G-T

174317456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56984646-A-G

http://identifiers.org/hco/4/GRCh38#174317501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56984606-C-A

174317509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56984598-A-G

174317509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56984598-A-T

174317588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56984531-T-A

174317588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56984531-T-C

174317588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56984531-T-G

174317731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56984383-T-C

174317773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56984341-A-G

174317819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56984295-A-G

174317824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56984290-T-A

174317860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56984268-A-G

174319246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56983686-A-G

174319253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56983679-G-A

174319367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 56983588-T-C

174319378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56983577-A-G

174319386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56983569-A-G

174319390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56983565-T-C

174319512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56983465-G-C

174319515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56983462-T-C

174319932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56982297-G-T

174319965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56982269-A-G

174320078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56982199-G-A

174320078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56982199-G-C

174320078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56982199-G-T

http://identifiers.org/hco/4/GRCh38#174320079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56982198-C-A

174320079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56982198-C-T

174320281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56982013-T-C

174320292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 56982002-T-C

174329568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56972066-C-G

174329605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56972029-G-A

174329853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56971793-G-A

174329922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56971732-C-T

174330057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56971708-C-G

174330061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56971704-C-G

174330922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56971505-G-A

174330995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56971393-T-C

174331005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 56971380-G-A

174331853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 56969825-T-G

174331979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 56969705-A-G

174332023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 56969667-G-C

174332023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 56969667-G-T

174332024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 56969666-A-G

http://identifiers.org/hco/4/GRCh38#174332063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56969626-C-A

174332063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 56969626-C-G

174332063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 56969626-C-T

174332097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 56969593-T-C

174332127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 56969583-T-C

http://identifiers.org/hco/4/GRCh38#174332153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56969558-C-A

174332153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 56969558-C-T

http://identifiers.org/hco/4/GRCh38#174332201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56969519-C-A

174332201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 56969519-C-G

174332251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 56969474-T-C

http://identifiers.org/hco/4/GRCh38#174332330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56969389-A-C

174332331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: 56969388-A-G

174332334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: 56969371-G-C

174332381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: 56969331-T-C

http://identifiers.org/hco/4/GRCh38#174332594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56969134-C-A

http://identifiers.org/hco/4/GRCh38#174332643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56969103-C-A

http://identifiers.org/hco/4/GRCh38#174332681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56969063-C-A

174332703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: 56969041-T-C

174332774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: 56968968-G-T

174332793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: 56968948-G-A

174332887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: 56968918-T-A

174332888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: 56968917-T-C

174332917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: 56968888-T-A

174332917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: 56968888-T-C

174332955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: 56968859-A-G

174332956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: 56968858-G-A

174332961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: 56968853-T-C

174332986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: 56968815-C-T

174333093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29356
most severe consequence: 3 prime UTR variant
orthologous variants: 56968705-T-C